| Title of Invention | HETEROCYCLIC METALLOCENE COMPOUNDS AND CATALYST SYSTEMS CONTAINING THE SAME |
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| Abstract | This invention relates to a metallocene compound of the general formula LGZMXp (I) (definition of these abbreviations are given in claim 1) This invention includes catalysst systems containing such metallocene compounds and a process for polymerization with such catalysts |
| Full Text | The present invention relates to a new class of metallocene compounds, to catalysts containing them and to a process carried out in the presence of said catalysts for the preparation of polymers of alpha-olefins, particularly propylene polymers, having a low degree of crystallinity. The present invention also relates to the ligands for those metallocenes and to a convenient process for their preparation: Products of propylene homopolymerization can have varying degrees of crystallinity. The type and amount of crystallinity is largely dependent on the microstructure of the polypropylene. Polypropylene having predominantly isotactic or syndiotactic structure is partially crystalline, while polypropylene having predominantly atactic structure is amorphous. Propylene polymers are also known which have a reduced degree of crystallinity and show elastomeric properties. U.S. patent No. 4,335,225, for instance, discloses a fractionable, elastic polypropylene, having an isotactic content of 55% or less, which contain a diethyl ether-soluble fraction with an isotactic crystalline content of about 0.5-5% by weight This polypropylene is prepared with a catalyst based on a tetraalkyl zirconium supported on a metal oxide. However, the elastomeric polypropylenes of this type, due to the fact that the catalyst systems which are used for their preparation have different catalytic sites, are endowed with a wide distribution of molecular weights which has a negative impact on their properties. Metallocene catalysts have recently been used in the polymerization reaction of olefins. Operating in the presence of these catalysts, polymers characterized by a narrow molecular weight distribution and having structural characteristics of interest have been obtained. By polymerizing propylene in the presence of metallocene catalysts, amorphous or highly crystalline polypropylenes can be obtained depending on the metallocene used Certain metallocene catalysts are also known that can produce partially crystalline elastomeric polypropylene. International application WO 95/25757, for instance, describes unbridged metallocene catalysts that can produce isotactic-atactic stereoblock polypropylenes having elastomeric thermoplastic properties. Despite the homogeneity in molecular weight distribution, the tacticity distribution of these polymers is not homogeneous. Moreover, the activity is low. U. Dietrich et aL in "J. Am. Chem. Soc. 1999,121, 4348-4355" describe metallocene catalysts that are able to produce thermoplastic elastic polypropylenes. More recently, heterocyclic metallocene compounds have been used in the polymerization of alpha-olefins. International application WO 98/22486 discloses a class of metallocenes containing a cyclopentadienyl radical directly coordinating the central metal atom, to which are fused one or more rings containing at least one heteroatom. These metallocenes, in combination with a suitable cocatalyst, are used in the polymerization of olefins such as propylene. The working examples relate to the preparation of highly stereoregular polypropylene. It would be desirable to provide a novel class of metallocenes which, when used in catalysts for the polymerization of olefins, in particular propylene, are capable of yielding polymers endowed with high molecular weights, narrow molecular weight distribution and a reduced degree of crystaUinity. fi would be most desirable to provide metallocene catalysts that can produce those polymers with high activity, such that the amount of catalyst remaining in the formed polymer is minimized. A novel class of metallocene compounds has now been unexpectedly found, which achieves the above and other results. According to a first aspect the present invention provides a metallocene compound of general formula (T): LGZMXp (0 wherein L is a divalent group bridging the moieties G and Z, selected from CR R, SiR R and (CRlR2)2, R1 and R2, which may be the same as or different from each other, are selected from hydrogen, a CrC20-alkyi, C3-C20-cycloalkyl, C2-C2cra]kenyl, C6-C20-aryl, Cr^o-a&ylaryl, C7-C20-arylalkyl radical, optionally containing heteroatoms belonging to groups 13-17 of the Periodic Table of the Elements, R1 and R2 can also form a ring having 3 to 8 atoms which can bear substituents; Z is a moiety of formula (D): i wherein R3 and R4, which may be the same as or different from each other, are selected from hydrogen, a C1-C20-alkyl, C3-C20-cycloalkyl, C2-C20-alkenyl, C^To-aryt C1-C20-alkylaryl, Cr-C^-aiylalkyl radical, optionally containing heteroatoms belonging to groups 13-17 of the Periodic Table of the Elements, preferably at least one of R3 and R4 being different from hydrogen; A and B are selected from sulfur (S), oxygen (O) or CR5, wherein R5 is selected from hydrogen, a Ci-Qo-alkyl, C3-C20-cycloa]kyl, Cr-Cao-alkenyl, CfCgroyl* C7-C20-alkylaryl, Cr-C20-aiylaDkyl radical, optionally containing heteroatoms belonging to groups 13-17 of the Periodic Table of the Elements, with the proviso that if A is S or O, then B is CR5 or if B is S or O, then A is CR5, Le. either A or B being different from CR5, and wherein the rings containing A and B have a double bond in the allowed position being two aromatic rings; G is a moiety of formula (HI): wherein R6, R7, Rs and R9, which may be the same as or different from each other, are selected from the group consisting of hydrogen, a Ci-C20-alkyl, C3-C20-cycloalkyl, C2-C20-alkenyl, Ce^o-aryi* CT-Czo-aHkyltaxyl, C7-C20-arylaIkyl radical, optionally containing heteroatoms belonging to groups 13-17 of the Periodic Table of the Elements, R6 and R7 and/or R8 and R9 can form a ring comprising from 3 to 8 atoms, which can bear substituents; with the proviso that R7 is different from R8 and when R7 is a tert-butyl radical R8 is not hydrogen; M is an atom of a transition metal selected from those belonging to group 3, 4, 5, 6 or to the lanfhanide or acthude groups in the Periodic Table of the Elements (new IUPAC version), X, same or different, is selected from a hydrogen atom, a halogen atom, a group R1Q, OR10, OSO2CF3, OCOR10, SR10, NR102 or PRl02, wherein the substituents R10 are selected from hydrogen, a Cl-C20-alkyl, C3-C20-cycloalkyl, C2-C20-alkenyl, C6-C20-aryl, CT-Czo-rikyteryl, Cy^o-arylalkyl radical, optionally containing heteroatoms belonging to groups 13-17 of the Periodic Table of the Elements; p is an integer from 0 to 3, preferably from 1 to 3, being equal to the formal oxidation state of the metal M minus 2; isopropyHdene(3-trimethylsilyicy^ dimethylsilanediyl(3-tiimeth^^ dichloride, isopropylidene (3-ethylcyclopentadienyl)(7K;^^ dichloride, dimethylsilanediyl (3-ethylcyclopentadieny^ dichloride, isopropylidene (3-n-butylcyclopenladienyl^^^ dichloride, dimethylsilanediyi (3-n4ratylcyclopemtadienyl)(7-^ dichloride, isopropylidene (3-metbyicyclopentadienyl)(7^^ dichloride, dimethylsilanediyl (3-methylcyclopmtadienyiX7^ dichloride, isopropylidene (3-i-propylcyclopentadienylX7-«^lo^ dichloride and dimethylsilanediyl (3-i-propylcyclopemiadienyl)(7-^^ dichloride being excluded. The transition metal M is preferably selected from titanium, zirconium and haftrium preferably having a formal oxidation state of+4. The X substituents are preferably chlorine atoms, benzyl or methyl groups. Preferably the bridging group L is a CMe2 or SiMe2 group. Preferably A or B is a sulfur atom and the other is a CH group, more preferably A is sulfur and B is a CH group. Preferably R3 and R4 are the same and are selected from a Ci-C20-alkyl group, which can contain a silicon atom. Most preferably R3 and R4 are a methyl, an ethyl, a phenyl or a trimethylsilyl radical. Non-limiting examples of metallocene compounds according to the present invention are: methylene(3-methyteyclopentadi^ dithiophene)zirconium dichloride and dimethyl; me1hylene(3-ethylKyclopentad^ dithiophene)zirconium dichloride and dimethyl; methylene(34sopropyl^yclopentadieny^ dithiophene)zirconium dichloride and dimethyl; me&ylene(3-phenyl-cyclopentadien^ dithiophene)zirconium dichloride and dimethyl; methylene(2,4-dmethyl-cyclopentadi dithiophene)zircomum dichloride and dimethyl; mdhylene(2,4-diethykyclop^ dithiophene)zirconium dichloride and dimethyl; methylene(2>4-diisopropyl-cycto dithiophene)zirconium dichloride and dimethyl; methylene(23>5-trimethyl^clopen^ ditMophene)zirconium dichloride and dimethyl; methylene(23>5-trie1hyl-cyclopenta&^^ di1hiophene)zirconium dichloride and dimethyl; methylene(23»5-triisopropyl-cyclopenta&^ b'] dithiophene)arconiuni dichloride and dimethyl; methylene(3- me&ylene-l-(todenyl>7-(2,5^met^^ dichloride and dimethyl; methylene-l-(indenyl>7-(2,5-ditrimethylsilylcyclopentadienyl-[l,2-h:4,3-b']dithiophene)zirconiuni dichloride and dimethyl; methylene-l-(3-isopropyl-indenyl)-7-(2,5-dimetiiylcyc]opentadieny]-[l,2"b:4,3-- b']dithiophaae)zirconium dichloride and dimethyl; methylene-1 -(34er-butyl-indenyl)-7-(2,5-dimethylcyclopentadienyl-[ 1 ,2-b :493- b,]dithiophene)zirconium dichloride and dimethyl; methylene:l-(23-dimethyl-indenyl)-7-(2,5-dimethylcyclopente b,]dithiophene)zirconiiim dichloride and dimethyl; methylene-1^3-methyl-indQQyl)-7-(2,5-dime1hylcyclopentadienyl-[l,2-b:43-b']dithiophene)zirconium dichloride and dimethyl; methylene-l-(tetrahy b']dithiophene)zirconium dichloride and dimethyl; methylene(3-methyl-cyclopentadienyl>7-(2,5-dimethylcyclopentadienyl-[l^ dioxazol)zarcomum dichloride and dimethyl; methylene(3-ethyl methylene(3-isopropyl-cyclopentadienyl)-7K2^^ dioxazol)zirconium dichloride and dimethyl; methyiene(3-phenyl-cyclopentadienyl>^^ dioxazol)zirconium dichloride and diinethyl; methylene(2,4- methyiene(2,4Hchethyl^clopentadieny dioxazol)zircotumn dichloride and dimethyl; methylene(2-niiethyi^phe^^ b'] dioxazol)zirconium dichloride and dimethyl; methylene(2,4-diiMpropyl- b']dioxazol)ziifconium dichloride and dimethyl; methylene(2,3,5-trimethyl-cyclopenta& dioxazol)zircoimnn dichloride and dimethyl; methylene(2^ ,5-triethyl-cyclopenta&^ dioxazol)zirconiiim dichloride and dimethyl; methylene(2,3,5-triisopropyl-cyclopenta^ b'] dioxazol)zirconium dichloride and dimethyl; methylene(3^clohexyl-cyclopentadienyl)-7-(2,5-dimethylcyclopentadienyl-[l,2-b:43-b'] dioxazol)zirconium dichloride and dimethyl; methylene-1 -(indenyl)-7-(2,5-dimethylcyclopentadienyl-[l ,2-b:4,3-b']dioxazol)zirconium dichloride and dimethyl; methylene-l-(2Lme1hyl-mdenyl>^ b']dioxa2ol)ziiconium dichloride and dimethyl; methylene-l-(23-dimdhyl-indenyl)-7-(2,5-dimethylcyclopentadienyl-[ 1 >2-b:4,3- b']dioxazol)ziiconium dichloride and dimethyl; methylene-Httfrahydromdenyl^ dioxazol)zirconium dichloride and dimethyl; methylene(3-methyl-cyclopen^ dioxazol)zircomum dichloride and dimethyl; methylene(3-isopropyl-cyclopentadi^ b'] dioxazol)zitcomum dichloride and dimethyl; methylene(3-methyl^yclopentadieny^ dioxazol)hafimun dichloride and dimethyl; isopropyMene(3-methyl-cyclopentadien^ dithiophene)zircoiiium dichloride and dimethyl; isopropyhdene(3-ethyl-cyclopentadienyl)-7-(2,5Kl^ dithiophene)zirconium dichloride and dimethyl; isopropyUdene(34sopropylK^clopentadienyl)-7-(2?5-dimeihylcyclopentadienyl- dithiophene)zirconium dichloride and dimethyl; isopropyhdene(3-phenyl-cyclopentadienyl)-7-(2,5-dimethyl dithiophene)zirconium dichloride and dimethyl; iscpropyhdene^^dimethyl^yclopentadim^ difliiophene)zirconium dichloride and dimethyl; isopropyhdene(2,4Kiimethyl-cyclopen1^ 1 ,2- b:4,3-b'] dithiophene)zirconium dichloride and dimethyl; isopropyUdene(2,4^ethyl-^clopent^ dithiophene)zirconium dichloride and dimethyl; isopropyhdene(2,4-dusopropy!-cyclopenta^ b'] dithiophene)zirconium dichloride and dimethyl; isopropyhdene(2-methyi^phenyl^yd^ 1,2- b:4,3-b'] dithiophene)zirconrum dichloride and dimethyl; isopropyhdme(2-methyl^phenyl-cyd^ [l,2-b:4,3-b'3 dithiophene)zirconium dichloride and dimethyl; isopropyhdene(2-methyl^isopro^ 1J2- b:4,3-t>'] dithiophene)zirconium dichloride and dimethyl; isopropyhdene(23,5-trimethyl^yclopen^ b'J dithiophene)zirconium dichloride and dimethyl; isopropyMene(2,3,5Mriethyl-cyclopenta^ b5] dithiophene)zirconium dichloride and dimethyl; isopropyhdene(23,5-triisopropyi isopropyhdene(3-cyclohexyl^yclopen1a^ b'] dithiophene)2irconium dichloride and dimethyl; isopropyhdene(3-isopropyl-c^clopentadienyl)-7^ b:4,3-b'] dithiophene)zirconium dichloride and dimethyl; b:4,3-b'] dithiophene)zarconmm dichloride and dimethyl; dimethylsttandiyl(2^,54riethyl-cyclopenta^ b'] dithiophene)zirconium dichloride and dimethyl; dmethylsilandiyl(2,3,5-triisopr^^ b:4,3-b'] dithiophene)arconium dichloride and dimethyl; dmethylsilandiyl(3-cyclohe^ b'] dithiophene)zircomum dichloride and dimethyl; dimethylsilandiyi(3-trimethylsU^^ 1,2- b:4,3-b?] ditWophene)zircoiiiiim dichloride and dimethyl; dime&ylsUandiyM-(indenyl)-7-(2,5-dime b']dithiophene)2arconium dichloride and dimethyl; dimethylalandiyi-l-(3-me&yl-mde b']dithiophene)2drconium dichloride and dimethyl; dimethylsttandiyl-l-(2,3^iime&^^ b']dithiophene)zircomum dichloride and dimethyl; dimethylsilandiyl-1 -(3-e£hyl-indenyl)-7-(2,5-dimetiiylcyclopentadienyl-[l,2-b:43- b']dithiophene)zirconium dichloride and dimethyl; dimethyisilandiyl-l-(34sopTC^ b']dithiophene)zirconium dichloride and dimethyl; dimethylsilandiyl-l-(3-isopropyl-^ b']dithiophene)2drconium dichloride and dimethyl; dimethylsUandiyl-l-(34sopropyl-indenyl)-7-(2,5-ditrimethylsilylcy b,]dithiophene)zirconium dichloride and dimethyl; dimethylsUandiyl-1^3-methyl-indenyl)-7-(2,5-dimetbylcyclopentadienyl-[l^ b']dithiophene)hafiuinn dichloride and dimethyl; dimethylsilandiyM-(34ertbu^ b']dithiophene)zirconium dichloride and dimethyl; dimethykilaadiyl4~(tetrahydroinden^ b']dithiophene)zirconium dichloride and dimethyl; isopiopyHdene(3-methyi-cyclopentadienyl)-7-(2,^^ dioxazol)zircomum dichloride and dimethyl; isopropyUdene(3-ethyl-cyclope^ dioxazol)zircorm3m dichloride and dimethyl; isopn>pyUdme(3-isopropyl-cycto^ dioxazol)zirconhim dichloride and dimethyl; isopropyMene(3-phenyl-cyclopenta^ dioxazol)zirconium dichloride and dimethyl; isopropyhdene(2,4KiimethylK^ 1 ,2-b :4,3 - b'^ioxazol)zirconium dichloride and dimethyl; isopropyUdene(2,4^ethylK^lopent^ b5]dioxazol)zirconium dichloride and dimethyl; isc^ropylidene(2,4-diisopropyl-^^^ b']dioxazol)2drconium dichloride and dimethyl; isopropyhdene(2,3,5-trimethyl-cyclopentadieny^^ b5] dioxazol)zirconium dichloride and dimethyl; isopropyHdeme(2,3,5-trie1hyl-(^clopent^ b'] dioxazol)zirconium dichloride and dimethyl; isopropyUdene(2,3,5-triisopropylK^ b:4,3-b'] dioxazol)zirconium dichloride and dimethyl; iscyropyUdene(3-cyclohexyl-cyclopm ,2-b:4,3- b'] dioxazol)zirconium dichloride and dimethyl; isoprc^yhdene(3-isopropyl-cyclo^ dioxazol)zirconinm dichloride and dimethyl; isopropyUdene-l-(indenyl)-7-(2,5-dimetilylcyclopentadienyl-[l?2-b:4,3-b,] dioxazol)zirconium dichloride and dimethyl; isopropyhdene-1^3-methyi-indenyl)-7-(2>5-dimethylcyclopentadienyl-[l^-^ dioxazol)zirconimn dichloride and dimethyl; isopropyUdene-1^3-ethyl4ndenyl)-7-(2,5Kim dioxazol)zirconium dichloride and dimethyl; isopropyUd^e-1^3-isopropyl-mdenyl)-7»(2,5-dimethylcyclopentadienyl-[l,2-b;4 dioxazol)zirconium dichloride and dimethyl; isopropyhdeae-l-(34ert-butyHndra^ dioxazol)zirconium dichloride and dimethyl; isopropyHdene-lKtetrahydroindenyl)-7-(2,5-dimethylcy^ dioxazol)zirconium dichloride and dimethyl; isopropyhdene4-(tetrahydxoindenyl)-7^ dioxazol)hafoium dichloride and dimethyl; dimethylsilandiyl(3-methyl^clopen^^ dioxazol)zirconium dichloride and dimethyl; dimethylsilandiyl(3-ethyl^clopeni^ dioxazol)zircomum dichloride and dimethyl; dimdhylsilandiyl(3-isopropyl^^lopen^ b'] dioxazol)zirconiiim dichloride and dimethyl; 'dimethylsttandiyl(3-phenyl dimethylsilandiyl(2,4-*iimethyl-c^ b'] dioxazol)zirconium dichloride and dimethyl; dimethylsilandiyl(2,4^ethyl-^ b'] dioxazol)zirconium dichloride and dimethyl; dmethylsUandiyl(2,4-diisopro b:4,3-b'] dioxazol)zirconiiim dichloride and dimethyl; dimethylsilandiyl(23,5-trimeth^^ b:4,3-b*] dioxazol)zirconiinn dichloride and dimethyl; dimethylsilandiyl(2,3,5-trie%lK;yclopentadienyl)-7^2,5-dm b'] dioxazol)zirconitim dichloride and dimethyl; dimethylsilandiyl(23,5-triisopro^ 1,2- b:4,3-b'] dioxazol)zirconium dichloride and dimethyl; dimetliylsilandiyl(3^yclohexyl dimethylsilandiyl(3-isopropyl^yclope^ b'] dioxazol)zirconium dichloride and dimethyl; dimethytelandiyl-l-(mdenyl>7^2^ dioxazol)zirconium dichloride and dimethyl; dimethylsilandiyi-l-(3-methyl-ind^^^ dioxazol)zirconium dichloride and dimethyl; dimethyisilandiyl-l-(2,3-dimethy^ dioxazol)zirconium dichloride and dimethyl; dime1hylsQandiyl-l-(3-isopK^^ dioxazol)zfrconium dichloride and dimethyl; dimethylsilandiyl-l-(tetrahyto dioxazol)zirconium dichloride and dimethyl; isopropyhdene(3-isopropyl-cyclopentadieny dithiophene)zdrconium dichloride; isopropyhdene(3-methyl-cyclopen^ dithiophene)zirconi1um dichloride; isopropyMene(3-methylK;yclopentadienyl)-7-^ dithiophene)hafinum dichloride; and dimethyl A particularly interesting class of bridged metallocenes of formula (T) according to the present invention is that wherein G is a moiety of formula (Ilia): wherein R6 and R9 equal to or different from each other, are selected from hydrogen, a C1-C20-alkyl, C3-C20-cycloalkyl, C2-C20-alkenyl, Ce-Qo-aiyl, C7-C20-alkylaryl, C7-C20-arylalkyl radical, optionally containing heteroatoms belonging to groups 13-17 of the Periodic Table of the Elements, preferably R6 is hydrogen and R9 is different from hydrogen; R7 is selected from a C6-C20-aryl, C7-C20-alkylaiyl or a QR11R12R13 group, wherein Q is selected from C, Si, Ge; R11, Ru and R13, which may be the same as or different from each other, are hydrogen, Ci-C20-alkyl, C3-C2 the Elements, with the proviso that when Q is a carbon atom, at least one ofRn,R12andR13 isa hydrogen atom. Particularly preferred metallocenes of the above mentioned class are those wherein R7 is selected from a phenyl group, a CHRnR12 group and a SiR11R12R13 group, R11, R12 and R13 being hydrogen or C1-C20-a&yI groups. Most preferred are those metallocene wherein QR11R12R13 is an isopropyl or a trimethylsilyl group. Non-limiting examples of this class of metallocenes are: isopropyHdene(3-isopiopyl^clope dithiophene)zirconium dichloride; isopropyhdene(3-methylH:yclopentedienyI)-^ dithiophene)zirconium dichloride; dimethylsilandiyl(3-ti^ethyk^ 1 >2~ b:4,3-b,]-dithiophene)zirconium dichloride; isopropyhdene(2-methyl^isopropyl-cyclopenta^ b:4,3-b']-dithiophene)zirconium dichloride; isopropytfdene(3-isopropyl-cyclopent b:4,3-b,]-dithiophene)zirconium dichloride; isopropyhdene(3-isopropyl^yclopent^ dithiophene)zirconium dichloride; isopropyhdene(2-methyM-phenyl-c^^ 1,2- b:4,3-b,]-ditihiophene)zirconium dichloride; isopropyMme(3-phenyl^yclopentadienyl)-7-(2^^ dithiophene)zirconium dichloride; isopropyhdene(2-methyl^phenyl-cy^ [l,2-b:453-b']-dithiophene)zirconium dichloride; isopropyMene(2,4-dimethyl^yclopentadiOT^ 1,2-b :4,3- b']-dithiophene)zirconium dichloride; isopropyHdene(2,4-dimethy]K;yclopen^ b:4,3-b']-dithiophene)zirconium dichloride; dimethylsttandiyl(2,4-^lime^ b']-dithiophene)zirconium dichloride;and isopropyKdene(3-metkyl^y^^^ dithiophene)ha&iuzn dichloride. Another advantageous class of bridged metallocenes of formula (I) is that wherein G is a moiety of formula (TV): wherein T1 is a sulfur atom or a CR16 group; T2 is a carbon atom or a nitrogen atom; z is 1 or 0; the ring containing Tl and T2 has double bonds in the allowed position; with the proviso that if z is 1, T1 is a CR16 group and T2 is a carbon atom and the ring formed is a benzene ring; and if z is 0, T2 bonds directly the cyclopentadienyl ring, the 5 membered ring formed has double bonds in any of the allowed position having an aromatic character and T1 and T2 are not at the same time, a sulfur atom and a nitrogen atom. R14, R15, R16, R1^ R18 and R19, the which may be the same as or different from each other, are selected from hydrogen, a Ci-Cao-alkyl* C3-C20-cycloalkyl, C2-C20-alkenyl, Q-Qo-aryl C7-C20-attylaryi, Cr^o-arylalkyl radical, optionally containing heteroatoms belonging to groups 13-17 of the Periodic Table of the Elements, and any of two adjacent R14, R15, R16, R17, R18andR19 can form a zing comprising 4 to 8 atoms which can bear substituents. An advantageous subclass of compounds belonging to the above class is that wherein G is a moiety of formula (IVa): wherein Ru, R15, R16, R17, R18 and R19, which may be me same as or different from each other, are selected from hydrogen, a Ci-C20-aIkyl, CrC& adjacent R14, R15, R16, R17, R18 and R19 can form a ring comprising 4 to 8 atoms which can bear substituents and the benzene ring can be perfcydrated. Non-limiting examples of metallocenes belonging to this class are: dimethylsilandiyl-l-(indenyl)-7-^ dithiophene)2irconium dichloride; dimethylsilandiyl-1 -(2-methyl-indenyl)-7-(2,5-dimethyl-cyclopentadienyl-[ 1,2-b:4,3-b' ]- dithiophene)rirconium dichloride. A preferred structure of compounds of formula (IVa) has the formula (TVb): wherein R15, R16, R17, and R18 are selected from hydrogen, a Ci-C20-alkyl, C3-C20-cycloalkyl, C2-C20-alkenyl, C6-C20-aryl C7-C20-alkylaiyl, C1-C20-arylalkyl radical, optionally containing heteroatoms belonging to groups 13-17 of the Periodic Table of the Elements, and any of two adjacent R14, R16, R17 and R18 can form a ring comprising 4 to 8 atoms which can bear substituents; R14 is selected from the group consisting of Ci-C20-alkyl or C6-C20-aryl group such as a methyl, ethyl, or phenyl group; Preferably when G is a moiety of formula (IVb) L is a group SiR R * wherein R and R have the * meaning described above, more preferably L is SiMe2. A further preferred structure of compounds of formula (IVa) has the formula (IVc) wherein R14, R16, R17, and R18 are selected from hydrogen, a Ci-C20-alkyi, C3-C20-cycloalkyl, C2-C20-alkenyl C6-C2 two adjacent R14, R16, R17, R18 and R19 can form a ring comprising 4 to 8 atoms which can bear substituents; R19 is selected from the group consisting of C]-C20-alkyl or Cg-Cao-aryl group such as a methyl, ethyl, or phenyl group or forms with R18 a benzene ring that can bears substituents. Preferably R14 is selected from the group consisting of Ci-C20-a]kyi or C6-C20-aryI group such as a methyl, ethyl, or phenyl group; preferably R16 is selected from the group consisting of Ci-C20-a&yl or C6-C2craiyl group such as a methyl, ethyl, or phenyl group Preferably when G is a moiety of formula (TVc) L is a group SiR^2, wherein R1 and R2 have the meaning described above, more preferably L is SiMe2. Another advantageous subclass of compounds wherein G is a moiety of formula (TV) is that wherein G is a moiety of formula (TVd) wherein: T1 is a sulfur atom or a CR16 group; T2 is a carbon atom or a nitrogen atom; the 5 membered ring formed by T1 and T2 has double bonds in any of the allowed position, having an aromatic character, with the proviso that if T1 is a sulphur atom T2 is not a nitrogen atom; R14, R17 and R18 which may be the same as or different from each other, are selected from hydrogen, a Ci-C20-alkyU C3-C20-cycloa]kjd, Cr-C20-aIkenyl, C6-C20-aryl, Cr-C20-alkylaiyI5 C7-C20-arylalkyl radical, optionally containing heteroatoms belonging to groups 13-17 of the Periodic Table of the Elements, and R17and R18 can form a ring comprising 4 to 8 atoms which can bear substitoents. Particularly preferred are those compounds wherein T2 is a carbon atom; Tl is sulphur and R14, R17 and R18 equal to or different from each other are Ci-Car-alkyl, Ce-C2(raryi; preferably R14, R17 and R18 are methyl or phenyl groups. Preferably when G is a moiety of fonnula (TVd) L is a group SiR3R2, wherein R1 and R2 have the meaning described above, more preferably L is SiMe2 According to another aspect of the present invention there is provided a class of ligands of formula (V): LG'Z' (V) wherein L is defined as described above; Z' is a moiety of formula (VI): and its double bond isomers; wherein A, B, R3 and R4 are defined as described above and the double bonds are in any of the allowed position; G' is a moiety of formula (VTT): and its double bond isomers; wherein R6, R7, R8 and R9 have the meaning as defined above. The ligand of formula (V) can be prepared according to the procedure known in the art, in particular when R4 and R3 are both hydrogen the ligand of formula (V) can be prepared as described in WO 98/22486. According to a iurther aspect of the present invention a process is provided for the preparation of a ligand of formula (V) comprising the following steps: a) contacting a compound of the formula (VHI) with a base selected from the group consisting of metallic sodium and potassium, sodium and potassium hydroxide and an organolithium compound, wherein the molar ratio between the compound of the formula (VHI) and said base is at least 1:1 wherein A, B, R3 and R4 are described above; b) contacting the obtained anionic compounds of formula (VIII) with a compound of formula (IX): wherein L, R6, R7, R8 and R9 are defined as above and Y is a halogen radical selected from the group consisting of chloride, bromide and iodide, preferably chlorine and bromine. When L is CR*R2 the ligand of formula (V) can be obtained by an alternative process comprising the following steps: a) contacting a compound of the formula (VEQ) with a base selected from the group consisting of metallic sodium and potassium, sodium and potassium hydroxide and an organolithium compound, wherein the molar ratio between the compound of the formula (Vm) and said base is at least 1:1; b) contacting the obtained anionic moiety of the formula (VI) with a compound of formula (X): wherein R1, R2, R6, R7, R8 and R8 have the meaning as defined above; and then treating the obtained product with a protonating agent The base used in step a) of both processes is preferably methyilithium or n-butyllithium. Preferably the protonating agent used in the above process is a quaternary ammonium salt and most preferably the protonating agent is ammonium chloride. Non limiting examples of the compound of formula (X) is selected from 6,6-dimethyifulvene and 3-isopropyl-6,6-dimethylfulvene. Non-limiting examples of compounds of formula (DC) ' are (3-methyl- cyclopentadienyl)dimethylchlorosilane, (3-isopropyl-cyclopentadien)i)dimethyl chlorosilane, l-(3-methyl^clopentadienyi)-14 and l-(3-isopropyl- cyclopentadienyl)-1,1 -dimethyl-2^-dimethyl-2-chloro-efliane. The compound of formula (VTS) in the case where B is a CR5 can be obtained by a process comprising the following steps: i) treating a compound of formula (XT): wherein A is sulfur or oxygen, with a compound of formula (XII): wherein A is sulfur or oxygen, ii) contacting the thus obtained product with a reducing agent in a molar ratio between said reducing agent and the product obtained under i) of at least 1; ili) contacting the product obtained under ii) with a compound selected from an organolithium compound, sodium and potassium in a molar ratio between said compound and the product obtained in step ii) of equal to or greater than 2; iv) treating the thus obtained product with an agent selected from the group consisting of copper chloride, copper iodide and Mg/Pd., in order to obtain a compound of general formula (XDT): When B is sulfur or oxygen and A is a CR5 group the compound of formula (Vm) can be obtained according to the process comprising the following steps: i) contacting a compound of formula (XIV): whereinB is sulfur or oxygen, with a compound of formula (XV): wherein B is sulfur or oxygen, and subsequently treating with a neutralization agent; ii) treating the thus obtained product with a reducing agent in a molar ratio between said reducing agent and the compound obtained under i) of at least 1; iii) contacting the thus obtained product with a mixture of an organolithium compound and tetramethylethylenediamine (TMEDA) in a molar ratio between said mixture and the product obtained under ii) of at least 2, iv) contacting the thus obtained product with an agent selected from the group consisting of copper chloride, copper iodide and Mg/Pd., in order to obtain a compound of formula (XVI): An alternative process for preparing the compound of formula (VIII) when A is S or O comprises the following steps: i) contacting an equimolar mixture of compounds of formulae (XVII) and (XVID): wherein A are sulfur or oxygen, with a Lewis acid or a mixture of a Lewis acid and aprotonic acid; ii) treating the thus obtained product with CH2O in a molar ratio between said mixture and CEfcO within a range between 10:1 and 1:10; hi) contacting the thus obtained product with a compound selected from an organolithium compound, sodium and potassium; iv) contacting the thus obtained product with an agent selected from the group consisting of copper chloride, iodine and Mg/PcL, in order to obtain a compound of general formula (XHT). The Lewis acid used in the above process is preferably selected from zinc dichloride, cadmium dichloride, mercury dichloride, tin tetrachloride, trifluoroborane, zirconium tetrachloride and titanium tetrachloride. Most preferably, the Lewis acid is zinc dichloride. The agent used in the above processes of the invention is preferably copper chloride. Preferably the reducing agent is a mixture of AICI3/L1AIH4. The organic lithium compound used above is preferably butylHthium. Another alternative process for preparing the compound of formula (VET) when A is S or O comprises the following steps: i) contacting a compound of formula (XDQ: with a base selected from an organolithium compound, sodium or potassium; treating the obtained product with a formic ester, wherein the molar ratio between said ester and the compound of formula (XK) is at least 1:2, and subsequently treating the obtained product with a reducing agent in order to obtain a compound of formula (XX): ii) contacting the compound of formula (XX) with a base selected from an organolithium compound, sodium or potassium and subsequently treating the dimetallated compound with an alkylating agent to obtain the compound of formula (XXI); or alternatively treating the dimetallated compound with an ester of boric acid and a protonating agent in order to obtain the compound of formula (XXH): and subsequently contacting with a mixture of an alkylating agent in the presence of an transition metal complex compound for obtaining the compound of formula (XXT); iii) contacting the alkylated compound obtained by step b) with a coupling agent; in order to obtain the compound of formula (XET). Preferably the alkylating agent is selected from dimethyisulphate (M^SCU), trimethylchlorosilane (MeaSiCI) and a mixture of compounds of formulae R3y and K^Y', wherein R and R are defined as above and Y' is selected from chloride, bromide and iodide, preferably Y* is a chlorine. Preferably the transition metal complex compound is PdC^ (dppf). In the above-described processes the reducing agent is preferably a mixture of AlCls/IiAltLi or a mixture of triethylsilane (EtsSiH) and CF3COOH. The preferred the base is butylHthium. Preferably the organic acid ester is an ester of formic acid. Preferably the coupling agent is selected from the group consisting of copper chloride, copper iodide and Mg/Pd. All the reactions are earned out in aprotic solvents. Non limiting examples of aprotic solvents suitable for the above reported processes are tetrahydrofurane, dimethoxyethane, diethylether, toluene, dichloromethane. pentane, hexane and benzene. During the whole process, the temperature is generally kept between -100°C and 80°C, preferably between -20°C and 40°C, Compounds of formula (V) can be suitable used as intermediates for the preparation of metallocenes of formula (I). Therefore, a still further aspect of the present invention is a process for the preparation of a metallocene compound of formula (I), obtainable by contacting the ligand of general formula (V), with a compound capable of forming the corresponding dianionic compound and thereafter with a compound of general formula MXp+2> wherein M, X and p are defined as above. The compound able to form said corresponding dianionic compound is selected from the group consisting of hydroxides of alkali- and alkaline-earth metals, metallic sodium and potassium, and organometallic lithium salts. Preferably, the compound able to form said corresponding dianionic compound is butylithium. Non-limiting examples of compounds of formula MXp+2 are titanium-, zirconium- and hafnium tetrachloride. More specifically, the ligand of formula (V) is dissolved in a polar aprotic solvent and to the obtained solution is added a solution of an organolithium compound in an apolar solvent. The thus obtained anionic compound is optionally separated, dissolved or suspended in a polar aprotic solvent and thereafter added to a suspension of the compound MXpf2 hi a polar aprotic solvent. At the end of the reaction, the solid product obtained is separated from the reaction mixture by techniques commonly used in the state of the art such as filtration or recrystallizatiotL Non limiting examples of polar aprotic solvents suitable for the above reported processes are tetrahydrofurane, dimethoxyethane, diethylether and dichloromethane. Non limiting examples of apolar solvents suitable for the above process are pentane, hexane, benzene and toluene. Throughout the process, the temperature is generally kept between -100°C and 80°C, preferably between -20°C and 40°C. ix the case in which at least one substituent X in the metallocene compound of the formula (I) is different from halogen an alternative process for preparing it consists in preparing the dihalogen derivative, i.e. the complex wherein both X substituents are halogen, and then substituting the halogen atoms with the appropriate X groups by the methods generally appllied. For example, if the desired substituents X are alkyl groups, the metallocenes can be made by reaction with alkylmagnesium halides (Grignard reagents) or with alkyllithium compounds. General methods for substituting X with substituents other than halogen such as sulfur, phosphorus, oxygen, etc. are described in Chem. Rev. 1994,94,1661-1717, and the cited references therein-According to a still further aspect of the present invention a catalyst for the polymerization of alpha-olefins is provided, obtainable by contacting: (A) a metallocene compound of formula (T) LGZMXp (I) wherein L, Z, M, X, and p has been defined above and G is a moiety of formula (HI): wherein R6, R7, R8 and R9, which may be the same as or different from each other, are selected from the group consisting of hydrogen, a Ci^Qo-alkyi, Cs-Cao-cycloalkyl, C2~C20-alkenyi> QK^o-aryl, CV^o-alkylaryl, C1-C20-aryla]kyl radical, optionally containing heteroatoms belonging to groups 13-17 of the Periodic Table of the Elements, R6 and R7 and/or R8 and R9 can form a ring comprising from 3 to 8 atoms, which can bear substituents; with the proviso that R7 is different from R8 and when R7 is a tertbutyl radical R8 is not hydrogen; and (B) an alumoxane and/or a compound capable of forming an alkyl metallocene cation. Preferably in the metallocene compound of formula (I) G is a moiety of formula (Ilia) or (TV), more preferably G is a moiety selected from the compound of formula (Ilia), (IVb), (IVc) or (IVd). The alumoxane used as component (B) can be obtained by reacting water with an organo-ahnninium compound of formula HjAlR23^ or HjAfcR23^, where R23 substituents, same or different, are hydrogen atoms, Ci-C20-alkyl, C3-C20-cyclalkyl, Q-C^-aiyl, Cr-C^-alkyiaryl or C7-C20-arylalkyl, optionally containing silicon or germanium atoms with the proviso that at least one R is different from halogen, and J ranges from 0 to 1, being also a non-integer number. In this reaction the molar ratio of Al/water is preferably comprised between 1:1 and 100:1. The molar ratio between aluminium and the metal of the metallocene is comprised between about 10:1 and about 20000:1, and more preferably between about 100:1 and about 5000:1. The alumoxanes used in the catalyst according to the invention are considered to be linear, branched or cyclic compounds containing at least one group of the type: wherein the substituents R23, same or different, are described above. In particular, alumoxanes of the formula: can be used in the case of linear compounds, wherein n is 0 or an integer from 1 to 40 and the substituents R are defined as above, or alumoxanes of the formula: can be used in the case of cyclic compounds, wherein u is an integer from 2 to 40 and the R23 substituents are defined as above. Examples of alumoxanes suitable for use according to the present invention are methylalumoxane (MAO), tetra-(isobutyl)alumoxane (TIBAO), tetra pentyi)alumoxane (TTOAO), tetra«(2^-dimethylbutyl)alumoxane (TDMBAO) and tetra-(233- trimefhylbutyl)alumoxane (TTMBAO). Particularly interesting cocatalysts are those described in WO 99/21899 and in PCT/EP00/09111 in which the aDcyl and aryl groups have specific branched patterns. Non-limiting ©camples of aluminium compounds according to said PCT applications are: tiis(2,3,3-trimethyi-butyl)alunimium, tris(2,3-dimethyl-hexyl)aluminium, tris(2,3-dime&yl- butyl)aluminium, tris(2^-dimethyl-pentyl)aluminium, tris(2,3-dimethyl-hq>tyl)aluininium, tris(2-me%l-3«ethyl-pentyl)alumiirium, tris(2-me%l-3"Ctfayl-hexyl)almninium> tris(2-methyl-3- ethyI-hq>tyi)aJuminium, tefc(2-me&yl-3iH^ tris(2-ethyl-3-methyl- butyl)aluminium, tris(2-etfayl-3-methyl-pentyl)alimiinhimJ 1ris(2,3^ethyl-pentyl)alum^ 1ris(2-propyl-3-methyl-bu1yi)alumimiim, tris(24sopropyl-3-metiiyl-butyl)alimiiinuii^ tris(2-isobutyl-3-meftyl-pentyl)duminimii9 tris(2,3,3-trimetfa>i-pmtyl)alumiiiiuia, tris(2>33-trimethyl-bexyl)aliimiTmiTri> lris(2-ethy1-33-dTTneftyUhiity1)a1iiniiTiiiiTnJ tris(2-ethyl- 3,3'dimetfayl-pentyl)alurniniiim., tris(2-isq)ippyl-3^-dimetihyl-bii^ tris(2-tmne^ylsayl-propyl)aluminiiim> tris(2-methyl-3-phenyl-butyi)ahnniiri^ tris(2-ethyl-3- phenyl-butyl)aluminium, tris(23-dime&yl-3-phemyl-buty^^ tris(2-phenyl- propyl)duminium, tris[2^4-fhioro-phenyl>propyl]alimiiniigna tris[2-(4-diloro-plienyl> propyi]aluminium, tris[2^3-isoprop3d-phenyl)-propyi]aluTTiiTiiimi, tris(2-phenyi- butyl)aluminium, tris(3-me1fayi-2-phgayl-butyl)alinT)miiiTTi9 tris(2-phenyl-pentyl)alimiinium, tris^-^entafluorophenyl^propyyaluiiiiiiium;, tris[2,2-diphenyl-ethyl]aluminiiim and tris[2-phenyl-2-methyl-propyl]aluminium, as well as the corresponding compounds wherein one of the hydrocarbyl groups is replaced with a hydrogen atom, and those wherein one or two of the hydrocarbyl groups are replaced with an isobutyl group. Amongst the above aluminium compounds, trimethylaluminium (IMA), txiisobutyMumimum (TIBAL), tris(2A4-trimethyl-pentyl)aliiininium (TIOA), tris(23-^imethylbutyl)almninium (TDMBA) and tris(233-trimethylbutyl)aluminium (TTMBA) are preferred. Non-limiting examples of compounds able to form an alkylmetallocene cation are compounds of formula D*^", wherein D+ is a Bnansted acid, able to donate a proton and to react irreversibly with a substituent X of the metallocene of formula (I) and E" is a compatible anion, which is able to stabilize the active catalytic species originating from the reaction of the two compounds, and which is sufficiently labile to be able to be removed by an olefinic monomer. Preferably, the anion E" consists of one or more boron atoms. More preferably, the anion K is an anion of the formula BAi4W, wherein the substituents Ar which can be identical or different are aryl radicals such as phenyl, pentafluorophenyl or bis(trifluoromethyl)phenyL Tetrakis-pentafluorophenyl borate is particularly preferred. Moreover, compounds of the formula BAr3 can conveniently be used. Compounds of this type are described, for example, in the published International patent application WO 92/00333. Further, compounds of the formula RM'-O-M'R, R being an alkyi or aiyl group, and M5 is selected from an element of the Group 13 of the Periodic Table of the Elements (new IUPAC version). Compounds of this type are described, for example, in the International patent application WO 99/40129. The catalysts of the present invention can also be supported on an inert carrier. This is achieved by depositing the metallocene compound (A) or the product of the reaction thereof with the component (B), or the component (B) and then the metallocene compound (A) on supports such as, for example, silica, alumina, magnesium halides, styrene/divinylbenzene copolymers, polyethylene or polypropylene. The supportation process is carried out in an inert solvent such as hydrocarbon for example toluene, hexane, pentane or propane and at a temperature rangeing from 0°C to 100°C, preferably the process is carried out at room temperature. A suitable class of supports which can be used is that constituted by porous organic supports functionalized with groups having active hydrogen atoms. Particularly suitable are those in which the organic support is a partially crosslinked styrene polymer. Supports of this type are described in European application EP-633272. Another class of inert supports particularly suitable for use according to the invention is that of the olefin, particularly propylene, porous prepolymers described in International application WO 95/26369. A further suitable class of inert supports for use according to the invention is that of porous magnesium halides such as those described in International application WO 95/32995. The solid compound thus obtained, in combination with the further addition of the alkyialuminium compound either as such or prereacted with water if necessary, can be usefully employed in the gas-phase polymerization. According to a still further aspect of the present invention a process is provided for the preparation of polymers of alpha-olefins comprising contacting one or more alpha-olefins under polymerization conditions with a catalyst comprising the product obtainable by contacting: (A) a metallocene compound of formula (T) LGZMXp (I) wherein L, Z, M, X, and p has been defined above and G is a moiety of formula (EI): wherein R6, R7, R8 and R9, which may be the same as or different from each other, are selected from the group consisting of hydrogen, a Ci-Quralkyl, C3-C20-cycloalkyl, C2-C20-alkenyl, C6-C20-aryl* C7-C2(ralkylaryl, Cr^o-arylalkyl radical, optionally containing heteroatams belonging to groups 13-17 of the Periodic Table of the Elements, R6 and R7 and/or R8 and R9 can form a ring comprising from 3 to 8 atoms, winch, can bear substitoents; with the proviso that R is different fromR and when R is a tert-butyl radical R8 is not hydrogen; and (B) an alumoxane and/or a compound capable oT forming an aDcyl metallocene cation. Preferably in the metallocene compound of formula (T) G is a moiety of formula (Hla) or (IV), more preferably G is a moiety selected from the compound of formula (Hla), (TVB), (Wc) or (IVd). The process for the polymerization of olefins according to the invention can be carried out in the liquid phase in the presence or absence of an inert hydrocarbon solvent, or in the gas phase. The hydrocarbon solvent can either be aromatic such as toluene, or aliphatic such as propane, hexane, heptane, isobutane or cyclohexane. The polymerization temperature is generally comprised between -100°C and +100°C and, particularly between 10°C and +90°C. The polymerization pressure is generally comprised between 0,5 and 100 bar. The lower the polymerization temperature, the higher are the resulting molecular weights of the polymers obtained. The polymerization yields depend on the purity of the metallocene compound of the catalyst The metallocene compounds obtained by the process of the invention can therefore be used as such or can be subjected to purification treatments. The components of the catalyst can be brought into contact with each other before the polymerization. The pre-contact concentrations are generally between 0.1 and 10 mol/1 for the metallocene component (A), while they are generally between 2 and 10"8 mol/1 for the component (B). The pre-contact is generally effected in the presence of a hydrocarbon solvent and, if appropriate, of small quantities of monomer. In the pre-contact it is also possible to use a non-polymerizable olefin such as isobutene, 2-butene and the like. Further, the molecular weights of the polymer obtained, in particular of propylene homo or polymers, 1-butene polymers or ethylene homo or copolymers, are distributed over relatively limited ranges. The molecular weight distribution can be represented by the ratio Mw/Mn which, for the present polymers, is generally lower than 4, preferably lower than 3.5 and, more preferably, lower than 3. The molecular weight distribution can be varied by using mixtures of different metallocene compounds or by carrying out the polymerization in several stages which differ as to the polymerization temperature and/or the concentrations of the molecular weight regulators. One of the preferred alpha-olefins to be used in the polymerization process of the present invention is propylene. When propylene is polymerized and G is a moiety selected from the compound of formula (ma) and (Wb) a propylene polymer having a melting enthalpy and triads (mm) satisfying the relation: 30 moiety selected from the compound of formula (IVc), (IVd) the polymer obtained generally have a catalyst activity and/or intrinsic viscosity higher than those obtained with similar catalyst used in the prior art. For example in J. Am. Chem. Soc. 1998, 120, 10786-10787 isopropylidene{ (3-tertbutytoyclopentadienyl)-7^ 1,2-b:4,3- b']-dithiophene) }zirconium dichloride was used for polymerizing propylene, with a catalyst activity of only 13 Kgfrnmol oath. The polymers obtained generally have the triads (mm) satisfying the relation: 70 More interesting propylene polymers obtainable with the process described above are propylene polymer having the following characteristics: - triads (mm) satisfying the relation 30 - melting enthalpy (AH) The molecular weights of the above said propylene polymers can be quite high. Thus, the intrinsic viscosity can reach values of greater than 0.7 dl/g, preferably greater than 1 dl/g, more preferably greater than 2. The propylene polymers described above are endowed with good balance between optical properties, being quite transparent and elastomeric properties. Thus the polypropylene of the present invention has the following properties: - Haze (ASTM 2457) from 15% to 30% preferably fiom 20% to 30%; - Gloss (60°C) (ASTM 2457) from 60% to 95%, preferably from 70% to 85%; - Tensile modulus (ASTM D4065) from 1000 Mpa to 200 Mpa, preferably fiom 700 Mpa to 400 Mpa; - Elongation at break (ASTM D4065) fiom 300% to 900%, preferably from 500% to 700%; - Strength at bi^ (ASTM D638) fiom W^^^ The microstructures of polypropilene obtained by the process of the present invention, cover a range of commercial copolymers such as elastomeric, flexible, and random-like polypropylene, but with the difference that the melting point of the polypropylene of the present invention is always higher than the cited copolymer. Thus polypropylene of the present invention can easily replace these more expensive copolymers. The polymerization reaction of propylene acconding to the invention can be carried out in the presence of ethylene or of a C4-C10 alpha-olefin comonomer. Thus a further aspect of the present invention is a propylene copolymer containing from 0.1 to 30% by moles, preferably fiom 0.1 to 20% by moles, more preferably from 0.1 to 10% by moles, even more preferably from 0.1 to 5% by moles of units deriving fiom an olefin of formula CHr=CHR', R' being hydrogen, a C2-C20-alkyl or a Cg-Cir-ayl group, said propylene copolymer having the following characteristics: melting enthalpy triads (mm) of the polypropylene homosequences satisfy the relation: 30 preferably 55 The process according to the present invention is also suitable for obtaining ethylene homo and copolymers wherein the olefin comonomers can be alpha-olefins, cyclolefins or polyenes. Ethylene homopolymers having a remarkably high molecular weight are obtainable. In fact, with the process of the present invention it is possible to obtain ethylene polymers having intrinsic viscosity (LV.) values as high as 5.0 dl/g and even higher. In the copolymers obtainable with the process of the invention, the molar content of ethylene derived units is generally higher than 40%, and preferably it is comprised between 50% and 99%, and most preferably it is comprised between 80% and 98%. The molar content of alpha-olefin derived units is preferably comprised between 0% and 60% and, more preferably, between 1% and 50%, and most preferably between 2% and 20%. Non-limiting examples of alpha-olefins which can be used as alpha-olefins in the process of the invention are propylene, 1-butene, 1-pentene, 4-methyl-l-pentene, 1-hexene, 1-octene, 4,6- dimethyl-1-heptene, 1-decene, 1-dodecene, 1-tetradecene, 1-hexadecene, 1-octadecene, 1-eicosene and allylcyclohexane. Non-limiting examples of cycloolefins that can be used as comonomers in the process of the present invention are cyclopentene, cyclohexene and norbornene. The copolymers according to the invention can also contain units derived from polyenes. The content of polyene derived units, if any, is preferably comprised between 0% and 30mol% and, more preferably between 0% and 2Qmol%. The polyenes that can be used as comonomers in the copolymers according to the present invention are included in the following classes: non-conjugated diolefins able to cyclopolymerize such as, for example, 1,5-hexadiene, 1- 6-heptadiene, 2-methyl-l,5-hexadiene; dienes capable of giving unsaturated monomelic units, in particular conjugated dienes such as, for example, butadiene and isoprene, and linear non-conjugated dienes, such as, for example, trans 1,4-hexadiene, cis 1,4-hexadiene, 6-methyl-l,5-heptadiene, 3,7-dimethyl-l,6-octadiene, 1 l-methyl-l,10-dodecadiene, and cyclic non-conjugated dienes such as 5-ethylidene-2-norbomene The metallocenes of the present invention can also be used for the polymerization in gas phase of ethylene with alpha-olefins such as propylene, 1-butene, 1-pentene, 4-methyl-l-pentene, 1-hexene, 1-octene, 4,6-dimethyl-l-heptene, 1-decene, 1-dodecene, 1-tetradecene, 1-hexadecene, 1-octadecene, 1-eicosene and allylcyclohexane. In the case of ethylene/propylene copolymers, the product of the reactivity ratios ri as, wherein ri is the reactivity ratio of propylene anil T2 that of ethylene, is calculated according to the following formula: rir2=l + f(x+l)«(f+l)Oc+l),/2 wherein f = ratio between moles of ethylene units and moles of propylene units in the copolymer, and X=(PPP + PPE)/EPE. The molecular weight of the polymers can be varied by varying the type or the concentration of the catalyst components or using molecular weight regulators such as, for example, hydrogen. The tacticity of the polymer chain, Le. the distribution of the relative configuration of the tertiary carbons, is determined by NMR analysis as described by Rescom et al Ghent Rev. 2000,100, 1253-1345 and reference cited therein. The polymers of the invention are transformable into shaped articles by conventional material processing, such as molding, extrusion, injection etc. The polymers of the present invention can be used for the preparation of synthetic leather, roofing blends, geomembranes, transparent objects, foam beds, as additive for bitumen or as polymer support for pigments and/or colors in masterbatches. EXAMPLES General procedures. All operations were performed under nitrogen by using conventional Schlenk-line techniques. Solvents were purified by degassing with N2 and passing over activated (8 hours, N2 purge, 300 °C) AI2O3, and stored under nitrogen. w-BuLi (Aldrich) was used as received. The proton and carbon spectra of ligands and metallocenes were obtained using a Bruker DPX 200 spectrometer operating in the Fourier transform mode at room temperature at 200.13 MHz and 50.32 MHz respectively. The samples were dissolved in CDCI3, CD2CI2 or CeD5. As reference the residual peak of CHCI3 or CHDCI2 or CeHDs in the *H spectra (7.25 ppm, 535 ppm and 7.15 ppm, respectively) and the peak of the solvent in the 13C spectra (77.00 ppm for CDCI3) were used. Proton spectra were acquired with a 15° pulse and 2 seconds of delay between pulses; 32 transients were stored for each spectrum. The carbon spectra were acquired with a 45° pulse and 6 seconds of delay between pulses; about 512 transients were stored for each spectrum. CDC13 (Aldrich, 99.8 atom% D) and C6D6 (Aldrich, 99.6 atom% D) were stored under molecular sieves (4-5 A), while CD2CI2 (Aldrich, 99.8 atom%D) was used as received. Preparation of the samples was carried out under nitrogen using standard inert atmosphere techniques. The proton and carbon spectra of polymers were obtained using a Bruker DPX 400 spectrometer operating in the Fourier transform mode at 120°C at 400.13 MHz and 100.61 MHz respectively. The samples were dissolved in C2D2CI4. As reference the residual peak of C2DHCI4 in the *H spectra (5.95 ppm) and the peak of the pentad in the 13C spectra (21.8 ppm) were used. Proton spectra were acquired with a 45° pulse and 5 seconds of delay between pulses; 256 transients were stored for each spectrum- The carbon spectra were acquired with a 90° pulse and 12 seconds (15 seconds for ethylene based polymers) of delay between pulses and CPD (waltz 16) to remove *H-13C couplings. About 3000 transients were stored for each spectrum. GC-MS analyses were carried out on a HP 5890 - serie 2 gas-chromatograph and a HP 5989B quadrupole mass spectrometer. The intrinsic viscosity (LV.) was measured in tetrahydronaphtalene (THN) at 135°C. The melting points of the polymers (Im) were measured by Differential Scanning Calorimetry (D.S.C.) on an Perkin Elmer DSC-7 instrument, according to the standard method. A weighted sample (5-10 mg) obtained from the polymerization was sealed into aluminum pans and heated at 200°C with a scanning speed corresponding to 20°C/minute. The sample was kept at 200°C for 5 minutes to allow a complete melting, of all the crystallites. Successively, after cooling to 0°C with a scanning speed corresponding to 20°C/minute, the peak temperature was taken as crystallization temperature (Tc). After standing 5 minutes at 0°CS the sample was heated for the second time at 200°C with a scanning speed corresponding to 20°C/min. In this second heating run, the peak temperature was taken as the melting temperature (Tm) and the area as global melting enthalpy (AHf). The molecular weight distribution was determined by SEC on a WATERS 200 machine in trichlorobenzene at 135°C. The following abbreviations are used: aq. = aqueous THF = tetrahydrofuran Et20 = diethyl ether CH2CI2 - dichloromethane DMF=N,N-*Iimethylfcnmamide Me2SiCl2= dichlorodimethylsilane MeaSiCl = chlorotrimethylsilane CuCl2 = copper (H) chloride POQ3 = phosphorus oxychloride B(OMe)3 = trimethyl borate AICI3 - aluminium trichloride n-BuIi = normal butyllithinm Dpp£= diphenylphosphinoferrocene TMEDA = N,N,N' JN'-tetramefliylethylenediamine ZrCU " zirconium tetrachloride HfCU = hafaium chloride Th2Cp= 7H-cyclopenta[l,2-b:4,3-b']-dithiophene or 7H-thieno[3',2':3,4]- cyclopenta[b]thiophene MeTh2Cp - 2,5-dimethyl-7H-cyclopenta[l,2-b:4,3«b']-dithiophene EtTh2Cp = 2,5-diethyl-7H-cyclopenta[l^-b:4,3-b']-dithiophene PhTh2Cp = 2,5-diphenyl-7H-cyclopenta[l,2-b:4?3-b']-dithiophene AcOH = acetic acid (MeO)2CH2 - dimefhoxymethane PREPARATION OF THE UGAND PRECURSORS Synthesis of S^'-dibromo^'-dithienylmethanol A 2.5 M solution of n-BuLi in hexane (24.30 mL, 60.76 mmol) was added dropwise at -20°C to a solution of 15.00 g of 2,3-dibromothiophene (Aldrich, 98%, Mw = 241.94, d = 2.137, 60.76 mmol, *-BuLi:2,3-Br2thiophene = 1:1) in 90 mL of ether. The solution turned from pale yellow to yellow. After 1 h stirring at -20°C, 2.53 mL of ethylformate (Aldrich, 97%, Mw = 74.08, d = 0.917, 30.38 mmol, HCOOEt:2,3-Br2thiophene = 0.5:1) in 30 mL of ether was added dropwise. During the addition the solution turned from yellow to dark yellow. The reaction mixture was kept at -20°C for 15 min, then allowed to warm to room temperature and stirred for 20 h. The final pale orange suspension was poured at 0°C into acidic water (1.65 g of NBUC1 in 75 mL of water), the organic layer was separated out and the water layer extracted with ether (3 x 25 mL). The organic layers were collected, dried over Na2SC>4 and the solvents were removed under vacuum at 30-35°C to give an orange oil (9.52 g), which was characterized by GC-MS analysis and ^-NMR spectroscopy. Purity (by GC-MS) = 96.0%. Yield of the pure product - 85.0%. *H NMR (5, ppm, CDC13): 7.28 (d, 2H, J = 5.29 Hz, CH); 6.95 (d, 2H, J « 5.29 Hz, CH); 6.41 (s, 1H, CH); 2.86 (bs, 1H, CH). m/z (%): 356 (23) \M* + 4], 354 (42) \tt + 2], 352 (22) [M*], 339 (10), 337 (18), 275 (10), 273 (10), 194 (11), 193 (23), 192 (11), 191 (100), 177 (32), 166 (10), 164 (10), 121 (17), 111 (14), 84 (33), 83 (15), 82 (26), 81 (14), 69 (11), 45 (33), 39 (15). Synthesis of 393'-dihromo-292,-dithieuylmethane 9.45 g of 3,3'-dibromo-2,2'-dithienylmethanol obtained as described above (Mw = 354.09, 26.69 mmol considering starting material as 100% pure) were dissolved in 85 mL of dichloromethane in a 250 mL three-necked bottom flask under nitrogen atmosphere and 4.26 mL of triethylsilane (Aldrich, Mw = 116.28, d = 0.728,26.69 mmol) were added at 0°C. Then 2.06 mL of CF3COOH (Aldrich, Mw = 114.02, d = 1.48, 26.69 mmol) were added dropwise at 0°C to the stirred mixture. During the addition, the reaction mixture turned from dark orange to dark red. It was kept at 0°C for 15-20 mfa, then allowed to warm to room temperature and stirred for 3 h and 30 mm at the same temperature. After cooling to 0°C, potassium carbonate (Fluka, 3.69 g, Mw = 138.21, 26.69 mmol) was added to the dark red solution, and the resulting mixture was stiired for 30 min at room temperature and finally filtered on G4 frit. The residue on the frit was washed twice with CH2CI2 (2 x 20 mL) until colourless, while the filtrate was dried under vacuum at 45 °C for 3 h to give a dark red oil (9.07 g), which was analysed by GC-MS analysis and 1H-NMR spectroscopy. Purity (by GC-MS) = 79.9%. Yield of the pure product» 80.3%. 3-bromo-2^,-di1hienylmefliane (9.9 wt%.) and hexaethyldisiloxane (6.2 wt%.) were present as by-products. The product was used as such in the next step without further purification. ]H NMR (5, ppm, CDC13): 7.16 (d, 2H, J = 5.38 Hz, CH); 6.94 (d, 2H, J = 5.38 Hz, CH); 4.27 (s, 2H, CH2). m/z (%): 340 (28) [M* + 4], 338 (51) [M* + 2], 336 (26) [M*], 259 (55), 257 (51), 179 (15), 178 (100), 177 (43), 89 (16), 45 (10). Synthesis of 7H^clopenta[l^b:43-b']dithiophene A 2.5 M solution of n-BuLi in hexane (21.30 mL, 53.25 mmol) was added dropwise at -50°C to a solution of 8.99 g of S^'-dibromo^^'-dithienylmethane obtained as described above (Mw = 338.09, 26.59 mmol) in 75 mL of ether under nitrogen atmosphere in a 250 mL flask. After 1 h stirring at -50°C, the dark brown dilithium suspension was added slowly to a suspension of 7.26 g of CuCl2 (Aldrich, 98%, Mw = 13445, 52.92 mmol) in 50 mL of Et20. The reaction mixture was kept at -50°C for 30 min, allowed to warm to -20°C in 2 h 30 min and then allowed to reach 0°C in few minutes. Aliquots were taken after 30 min at -50°C, at -20°C and after 1 h at 0°C to follow the reaction state by GC-MS analysis. It appeared that the CuCb induced coupling reaction starts at -50°C but proceeds slowly until 0°C. Only 10wt% of TH-cyclopentaPjl-b^^-b^dithiophene was formed after 1 h at 0°C. After keeping at 0°C for 1 h 30 min3 the reaction mixture was stirred overnight at room temperature and subsequently poured at 0°C into 100 mL of an aqueous 2 M HC1 solution. The resulting mixture was stirred for 15 min at room temperature, filtered in order to remove the greysh precipitate of CU2CI2, the ether layer was separated and the aqueous phase extracted with ether. The combined ethereal extracts were washed with HC1 2 M (100 mL), twice with NaHCC>3 aq. and finally with ether. The resulting organic phase (final volume = 300 mL) was dried with Na2S04 and the solvents removed in vacuo giving 3.16 g of a dark red oil, which was analysed by GC-MS analysis and *H-NMR spectroscopy. The analysis showed the presence of the desired product together with dimers, trimers and tars. The crude product was added of 40 mL of ethanol and stirred for 1 h at room temperature. The yellow-orange extract was concentrated in vacuo at 55°C for 4 h to give a dark orange oil (1.92 g), which crystallized by standing at 0°C overnight Purity (by GC-MS) = ca. 50%. Yield of the pure product - 20,2%. *H NMR (8, ppm, CDC13): 7.30 (d, 2H, J = 4.93 Hz, CH); 7.13 (d, 2H, J - 4.93 Hz, CH); 3.80 (s, 2H, CH2). m/z (%): 180 (9) [M* + 2], 179 (16) [M* + 1], 178 (100) JM*]f 177 (92), 134 (13), 89 (7), 69 (6), 45 (6). Synthesis of bis(3^-dibromo-2-thienyl)methanoI (or 33'^'-tetrabromo-2;2'-dithieiiyl carbinol) A solution of 31,35 g of 2,3,5-tribromothiophene (Lancaster, 98%, MW = 320.84, 95.75 mmol) in 70 mL of ether was cooled to -78°C and 38.3 mL of a 2.5 M «-BuLi solution in hexane (95.75 mmol) were added dropwise. The resulting mixture was allowed to warm to room temperature, stirred in additional 1 h and then added at 0°C -s- -10°C to a solution of 3.86 mL of ethylformate (Aldrich, 97%, MW = 74.08, d = 0.917,46.35 mmol) in 20 mL of hexane, previously cooled to 0°C 4- -10°C. At the end of the addition (~ 20 min) the reaction mixture was allowed to warm to room temperature and then refiuxed for 1 h. The resulting mixture was quenched with 7.5 mL of water, the organic layer was separated out, dried over magnesium sulphate and the solvents evaporated off giving 23.2 g of a pale brown solid, which was analyzed by !H NMR, 13 C NMR, GC-MS. Purity = 93.0%. Isolated yield with respect to ethylformate = 90.9%. ]H NMR (5 in ppm, CDCI3): 6.92 (s, 2H, CH); 6.26 (d, 1H, CH bridge, J = 3.2 Hz); 2.73 (d, 1H, OH, J = 3.2 Hz) 13C NMR (8 in ppm, CDCI3): 67.38 (CHOH), 108.60,113.58,132.18 (CH), 141.10. m/z (%): 512 (67) \ht]9 494 (50), 433 (54), 352 (53), 335 (35), 285 (43), 269 (100), 242 (19), 162 (33), 81 (27), 39 (13). Synthesis of 393%595,-tetrabromo-292,Hiithienylmethane Trifluoroacetic acid (025 mL, Aldrich, 99%, MW = 114.02, d = 1.48,3.24 mmol) was added at room temperature to a solution of 1.75 g of bis(3,5-dibrcmio-2-thienyl)meflianol (93.0%, MW = 511.90, 3.18 mmol) in 15 mL of methylene chloride containing 0.50 mL of triethylsilane (Aldrich, 99%, MW = 116.28, d = 0.728, 3.13 mmol). The resulting red solution was stirred for 1 h at room temperature, neutralized with solid potassium carbonate (0.4 g, MW = 13821,2.89 mmol), filtered and evaporated off to give a pale red solid. Yield of crude product = 100%. ]H NMR (5 in ppm, CDC13): 6.94 (s, 2H, CH); 4.17 (s, 2H, CH2). l3C NMR (5 in ppm, CDC13): 29.30 (CH2), 109.07,111.38,131.98 (CH), 137.22. m/z (%): 496 (71) [M* + 4], 417 (76) [M*], 336 (91), 255 (100), 176 (41), 125 (46), 95 (30), 69 (40), 45 (22). Synthesis of 33'-dibromo-5^9-dimethyl-2,2'-dithienyImethane A precooled (-20°C) 2.5 M Solution of w-BuIi in hexane (41.1 mL, 102.75 mmol) was added at -20°C to a solution of 25.48 g of S^'^^^tetrabromo^^dithienylmethane (MW «' 495.90, 51.38 mmol) in 100 mL of Et20. After 30 min stirring at -20°C, a precooled (-20°C) ethereal (10 mL) solution of dimethyl sulphate (Aldrich, 9.72 mL, MW = 126.13, d « 1.333, 102.75 mmol) was added. The resulting black suspension was stirred for 45 min at - 20°C; the cooling bath was then removed and the flow of nitrogen stopped. A 4 N solution of sodium hydroxide (2.5 mL, 10 mmol) was added and the mixture vigorously stirred for 2 h at room temperature. The resulting reaction mixture was dried by magnesium sulphate, filtered, the residue on the frit washed twice with ether (to recover all the product) and the filtrate was concentrated under reduced pressure at 40°C for 2 h giving 17.8 g of a brown solid. Purity = 87.8% (by GC-MS). Yield of pure product = 83.1% (crude yield = 94.6%). !H NMR (8 in ppm, CDC13): 6.58 (q, 2H, CH, J = 1.0 Hz); 4.11 (s, 2H, CH2); 2.39 (d, 6H, CH3,J = 1.0Hz). l3C NMR (5 in ppm, CDCI3): 15.41 (CH3), 28.88 (CH2), 108.20, 127.57 (CH), 134.10, 138.70. m/z (%): 366 (43) [M4], 287 (47), 206 (100), 191 (21), 173 (14), 103 (10), 59 (20). Synthesis of 2,5-dimethyl-7H-cyclopenta[l^-b:43-b']dithiophene (or 2,5-dimethyl-7H- thienoP'^'rS^Jcyclopentapbjthiophene) A precooled (-70°C) 2.5 M n-BuLi solution in hexane (27.1 mL, 67.75 mmol) was added dropwise at - 70°C to a solution of 10.77 g of 3,3'-dibromo-5,5'-dimethyl-2^'-ditbienylmethane (MW = 366.15, 29.41 mmol) in 60 mL of ether. At the end of the addition, the brown suspension was stirred for additional 30 min at the same temperature. Then a precooled (-70°C) suspension of 10.28 g of CuCl2 anhydrous (dried at 130 °C for 1 h, MW = 134.45, 76.46 mmol) in 35 mL of ether was added quickly. The resulting black suspension was kept at - 70°C for 10 min, at - 50°C for 1 h, at - 20°C for 1 h and at 0°C for 1 h. Then it was allowed to warm to room temperature and stirred overnight. The colour of the reaction mixture was' changed from black to pale brown by increasing the temperature. Aliquots were taken during the reaction for the GC-MS analysis: at - 50°C titre of the desired compound = 8.6%, at - 20°C title in the desired compound = 20.9%, at 0°C title in the desired compound = 68.8%. The final suspension was poured into 160 mL of an ammonium chloride saturated aqueous solution, the organic layer was separated, the water layer washed with ether, the organic layers collected and dried. 4.79 g of a black solid was obtained. Purity (by GC-MS) = 75.9%. Yield of pure product = 60.0 % (crude yield = 79.0%). !H NMR (8 in ppm, CDCI3): 6.78 (s, 2H, CH); 3.69 (s, 2H, CH2); 2.54 (s, 6H, CH3) l3C NMR (8 in ppm, CDCI3): 15.96 (CH3), 33.13 (CH2), 116.43 (CH), 140.16, 142.16, 143.67. m/z (%): 206 (100) [M4], 191 (54), 173 (29), 158 (6), 147 (8). Synthesis of 33'-dibromo-5^'-ditrimethylsnyl-2,2'-dithienyhnethane A 2.18 M solution of w-BuLi (65 mL, 141.7 mmol) was added at -70°C to a solution of 34.8 g of 33%535'4etrabromo-2^-di1iiienylmethane (70.2 mmol) in 150 mL of ether. The mixture was stirred for 30 min at the same temperature and 35.5 mL of MeaSiCl (280 mmol) in 65 mL of ether were then added. The resulting mixture was allowed to warm to room temperature, the LiCl was filtered pf£ and the mother solution was evaporated off to give an oil which represented the target compound in at least 95% purity. To this oil 50 mL of hexane was added and the resulting solution kept at -30°C for 10 h. Large crystals were isolated, washed with cooled hexane and dried. Yield of recrystallized product 60%. The title compound was characterized by lH-NMR and l3C-NMR spectroscopy. Synthesis of 2?5-ditrimethylsilyl-7H-cyclopenta[l!^-b:43-b,]dithiophene (or 2,5-dimethyltrimethylsUyl-7H-thieno[3,^\'394]cydopentaj>]thiophene) A solution of 0.1 mol of S^'^bromo-S^^-ditximethykilyl^^^lMenylmetliane in 200 mL ether was treated with 0.23 mol of n-BuLi at -70°C. At the end of the addition, the reaction mixture was stirred for additional 30 min at the same temperature. Then 0.265 mol of CuCfe was added quickly. The resulting mixture was allowed to warm to room temperature and stirred overnight. The resulting suspension was poured into water, the organic phase was separated and concentrated. The residue was passed through a column packed with Si02 using hexane or a hexane/ether mixture as eluent The resulting solution was evaporated off giving a crystalline or oily-crystalline solid which represented the desired product Yield 50-60%. The crude product can be further purified in ether by filtration at 0°C or by recrystallization from pentane. The title compound was characterized by lH-NMR and X3C-NMR spectroscopy. Synthesis of 33'-dibromo-5^'-dihydroxyboryI-2^'-dithienyImethane A 1.6 N solution of n-BuLi (100 ml, 160 mmol) was added to a solution of 39.6 g of 3,3\5,5'-tetrabromo-2,2'-dithienylmethane (79.8 mmol) in 150 mL ether at -70°C. The mixture was stirred for 30 min at the same temperature and 23.3 g of B(OMe)3 (220 mmol) in 100 mL of ether were then added. The reaction mixture was allowed to warm to room temperature. The resulting suspension was treated with 100 mL of a 10% aqueous HC1 solution, the organic layer was separated, washed twice with. 50 mL of a aqueous Na2CC>310% solution, evaporated off and dried. The resulting solid which represented the crude di-boronic acid was used in the next step without further purification. The title compound was characterized by lH-NMR and 13C-NMR spectroscopy. Synthesis of 33,-dibromo-5,5'-diphenyl-2^2,-dithienylmethane 1.81*g of 3,3'Kiibromo-5,5'-dihydroxyboryl-2^'^thienylmefliane (3.76 mmol), 1.40 g of Phi (6.84 mmol), 0.15 g of PdCl2(dppf)2 (0.21 mmol), 120 mL of DMF and 8 mL of Et3N were placed into a reaction flask and this mixture was stirred at 80°C for 2 h. The resulting mixture was poured into a Cl^CVwater two-phase system. The organic layer was collected, washed twice with 30 mL of 10% phosphoric acid, then with water and finally evaporated off. The residue was passed through a column packed with SiQj using hexane/CIfcCh - 1/1 as eluent The resulting solution was evaporated of£ the residue washed with hexane and dried to give 0.6 g of diphenyl derivative. Yield 32%. The titie compound was characterized by !H-NMR and 13C-NMR spectroscopy. Synthesis of 295-diphenyI-7H-cyclopenta[l^-b:493-b']dithiophene (or 2,5-diphenyl -7H-thieno[3'^2':3,4]cyclopenta[b]thiophene) A 1.6 N n-BuLi solution (11.9 mL, 19 mmol) was added to a solution of 4.24 g of 3S3S-dibromo-5,5'-^phenyl-2^2'-ditibienylmethane (8.65 mmol) in 50 mL of ether at —70°C. At the end of the addition, the reaction mixture was stirred for additional 30 min at the same temperature. Then 5.6 g of CuCb (41.8 mmol) was added quickly. The resulting mixture was allowed to warm to room temperature and stirred overnight Hie final suspension was poured into water, the organic phase was separated and the solvent evaporated off. The residue was passed through a column packed with Si02 using hexane/CEfeCk — 4/1 as eluent The resulting solution was evaporated off to leave a residue, which was washed with hexane and dried to give 1.1 g of crystalline solid. Yield 38%. The title compound was characterized by !H-NMR and 13C-NMR spectroscopy. Synthesis of 2-methyl-4-bromo-thiophene 1 mol of 2-thiophenecarboxaldeihyde was added to 2.5 mol of pulverized AlCb under stirring keeping the temperature below 40°C. At the end of the addition the liquid complex was solidified; then 1.2 mol of bromine was carefully added dropwise under stirring. When the addition was complete, stirring became impossible because of the mixture solidified completely. This solid substance was poured into a mixture of ice (0.5 Kg) and hydrochloric acid (100 mL, 32%), then 300 mL of CH2CI2 was added. The organic phase was separated and the solvent removed. The resulting substance (4~bromo-2-thiophenecaiboxaldehyde) was dissolved in 700 mL of di(ethylene glycol) and the so-obtained solution was treated with 5.5 mol of hydrazine hydrate. The resulting mixture was refluxed for 30 min. After cooling up to room temperature, 2.75 mol of potassium hydroxide was added. After the gas evolution was over, the distillation was started and the fraction before 150°C was collected. This fraction represented the mixture of water and desired product: the organic layer was separated and distilled at 60°C/10 torr. Yield 52%. ]H NMR (5 in ppm, CDC13): 6.99 (d, 1H, Ha); 6.69 (q, 1H, Hp); 2.48 (d, 3H, CH3). Synthesis of 2-methyl-4-formyl-thiophene A 1.6 M solution of n-BuIi (164 mL, 0.26 mol) was added at -70°C to a stirred solution of 44.26 g of 2-methyl-4-bromo-thiophene (025 mol) in 300 mL of ether. The resulting solution was kept under stirring at -60°C * -70°C for 30 min and then was treated with 27.4 g of dimelhylfonnamide (0.37 mol) in 100 mL of ether. The mixture was allowed to wann to room temperature, then neutralized with 10% aqueous solution of NH4CI, washed with 10% aqueous solution of H3PO4 and finally with water up to neutral pH. The organic phase was collected, evaporated off and distilled at 110°C/10mmHg. Yield 22.3 g (71%). The title compound was characterized by ^-NMR spectroscopy. Synthesis of 2,2'-dimethyl-4,4'-dithienylmethane 113 mL of 1.6 M n-BuLA solution (0.18 mol) was added to a solution of 31.3 g of 2-methyl-4-bromo-thiophene (0.177 mol) in 150 mL of ether at -70°C under stirring. The resulting solution was kept under stirring at -60 * -70°C for 30 min and then was added of 223 g of 2-methyl-4-formyi-thiophene (0.177 mol) in 100 mL of ether. The mixture was allowed to warm to room temperature, then neutralized with 10% aqueous solution of NH4CI and washed with water. The organic phase was separated and evaporated. The crude bis(2-methyl-4-thienyl)methanol (or 2,2,-dimethyl-4,4'-dithienyl carbinol) was obtained. A suspension of 35.5 g of AICI3 (0.266 mol) in 100 mL of ether was added slowly to a suspension of 10 g of LLAIH4 (0.266 mol) in 100 mL of ether. The resulting mixture was treated with the solution of the carbinol (obtained as described above) in 100 mL ether. The reaction mixture was refluxed for additional 1 h, cooled to room temperature and subsequently added of 100 mL of ethyl acetate. Then it was treated with 300 mL of water and 300 mL of ether. The organic phase was collected, washed with water, dried by MgSC>4 and evaporated off. The residue was distilled at 90*110°C/0.5 mmHg. Yield 23.2 g (63%). The title compound was characterized by !H-NMR spectroscopy. Synthesis of 2,6-dimethyl-4H-cyclopenta[2?l-b:3,4-b,]dithiophene (or 2,6-dimethyl-4H- thieno[3y:2,3]cyclopeiita[b]thiophene) 1.04 g of 2,2'-dimethyM,4'-ditMenylmethane (5 mmol) was dissolved in 30 mL of ether and added of 9 mL of a 1.6 M solution of n-BuIi (14.4 mmol) and of 1.74 g of TMEDA (15 mmol) at -70°C under stirring. The resulting mixture was allowed to warm to room temperature, stirred for 1 h, then cooled again to -70°C and treated with 2.7 g of CuCh (20 mmol). The resulting reaction mixture was allowed to warm to room temperature and added of 30 mL of water. The organic phase was collected and passed through a column packed with silica gel. The resulting solution was evaporated off to give 0.34 g of the product. Yield 34%. The title compound was characterized by lH-NMR spectroscopy. Synthesis of 2-ethyl-4-bromo-thiophene 1 mol of acethylthiophene dissolved in 250 mL of CHCU was added slowly to a suspension of 2.5 mol of AICI3 in 1000 mL of CHCI3 under stirring keeping the temperature below 40°C. At the end of the addition, 1.2 mol of Br2 was carefully added dropwise under stirring. The resulting mixture was stirred overnight and then was poured into a mixture of ice (0.5 Kg) and hydrochloric acid (100 mL, 32%). The organic phase was isolated and the solvent was removed. The resulting substance was dissolved in 700 mL of diethyleneglicole and the so- obtained solution was treated with 5.5 mol of 100% hydrazine hydrate. The resulting mixture was refluxed for 30 min. After cooling to room temperature, 2.75 mol of KOH were added. When the gas evolution was ended, the product was distilled. The fraction under the temperature of 150°C was collected This fraction represented a mixture of water and product The organic layer was collected and distilled at 80°C/10 torr. Yield 45%. 'H-NMR (5, ppm, CDCI3): 7.05 (d, 1H, H5); 6.76 (q, 1H, H3); 2.86 (q, 2H, CH2); 1.33 (t, 3H, CH3). Synthesis of 3^9^bromo-5^'^ethyl-2^9-ditfaienylmethane The 2-ethyl-4-bromothioplieiie obtained in the previous step was dissolved into 120 mL of AcOH and was treated with a mixture of 6.1 mL of H2SO4 and 9.1 mL (MeO^CHa. The reaction mixture was stirred overnight, then was washed with 300 mL of water and finally extracted with CH2CI2. The organic phase was separated and dried under reduced pressure. The residue was passed throught a column packed with AI2O3 using hexane as etuent The solvent was removed and the desired product was obtained as yellow oil. Yield 90%. !H-NMR (8, ppm, CDCI3): 6.68 (m, 2H, CH); 420 (s, 2H, CH2 bridge); 2.80 (q, 4H, CH2); 1.30(t,6H,CH3). Synthesis of l^-diethyl-TH-cyclopentatljl-b^^-b'l-dithiophene A solution of 0.1 mol of S^'^bromo-SjS'^ethyl^^'-dithienylmethane in 200 mL of ether was treated at -70°C with 0.23 mol of n-BuIi. At the end of the addition, the mixture was stirred for additional 30 min at the same temperature. The white precipitate of the dilithium salt was formed. Then 0.265 mol of CuCfe was added quickly at -70°C. The reaction mixture was allowed to warm to room temperature and stirred for 12 h. The resulting suspension was poured into water, the organic phase was separated and concentrated. The residue was recrystallized from ether. Yield 25%. ^-NMR (8, ppm, CDCI3): 6.86 (m, 2H, CH); 3.74 (s, 2H, CH2); 2.98 (q, 4H, CH2); 1.38 (t, 6H,CH3). EXAMPLE 1 Synthesis of 2^^3-methylH^clopentadienyl)-7-(2^-dimethyl-cyclopenta [l,2~b:43-b']- dithiophene)propane 3.13 mL of a 1.6 M solution of w-BuLi (5 mmol) was added at -70°C to a solution of 1.03 g (5 mmol) of 2,5-dimethyl«7H^yclopenta[l,2-b:4,3-b']Hiithiophene in 20 mL of ether. The resulting mixture was stirred for additional 30 min at 0°C, then cooled again to -70°C and treated with 0.6 g (5 mmol) of 3,6,6-trimethylfulvene in 10 mL of efher. The reaction mixture was allowed to warm to room temperature and then treated with a saturated aqueous solution of NH4CI, The organic phase was isolated, dried by MgS(>4 and concentrated. The residue was recrystallized from hexane. Yield 1.0 g (62%). The title compound was characterized by lH-NMR spectroscopy. Synthesis of isopropylidenej (S-methyl-cyclopentadienyiyT^^-dimethyl-cyclopentall^-bz^-b'i-dithiophene) } zirconium dichloride C-l 2.3 mL of 1.6 M n-BuLi solution (3.7 mmol) was added at —70°C to a suspension of 0.6 g (1.85 mmol) of 2,2^3-methyl-cyclopentadieny^ dithiophene)propane in 20 mL of ether. The mixture was allowed to warm to 0°C and then was treated with 0.43 g (1.85 mmol) of ZrCU. The reaction mixture was refluxed under stirring for 3 h, then the yellow precipitate was filtered, washed twice with ether, dried and finally recrystallized from CH2CI2. Yield 0.72 g (80%). The title compound was characterized by ^-NMR spectroscopy. EXAMPLE 2 Synthesis of isopropylidene{ (3-methyl-cyclopentadienyI)-7-(2^-dimethyl- cycIopenta[l,2-h:4,3-b']-dithiophene) }hafnium dichloride CH-1 2.5 mL of 1.6 M «-BuLi solution (4.0 minol) was added at -70°C to a suspension of 0.65 g (2.0 mmol) of 2£-(3-me1hyl^clopenta& ^-b:4^3-b']- dithiophene)propane in 20 mL of ether. The mixture was allowed to warm to 0°C and then was treated with 0.64 g (2.0 mmol) of HfCU- The reaction mixture was refluxed under stirring for 3 h, then the yellow precipitate was filtered, washed twice with ether, dried and finally recrystallized from Cl^Cb- Yield 0.48 g (42%). The title compound was characterized by 1H- NMR spectroscopy. EXAMPLE 3 Synthesis of 2,2-(2,4-dimethyl-cyclopentadienyl>-7-(295-dimethyl-cyclopenta [l,2-b:4,3-b']- dithiophene)propane The same procedure described for the synthesis of 2,2-(3-methyl-cyclopentadienyl)-7-(2,5- dimethyl-cyclopenta [l^-b:4,3-b5]-dithiophene)propane was followed (see below). Synthesis of isopropylidene{ (2,4-dimethyl-cyclopentadienyl)-7-(2^-dimethyl- cyclopenta[l,2-b:4,3-b']-dithiophene) }zirconium dichloride C-12 3.13 ml of 1.6 M n-BuIi solution (5.0 mmol) was added at-70 °Cto a solution of 1.03 g (5.0 mmol) of 2,5-dimethyl-7H--cyclopenta[l>2-b:4,3-b,]dithiophene in 20 mL of ether. The resulting mixture was stirred for additional 30 min at 0°C, then cooled again to -70°C and treated with 0.67 g (5.0 mmol) of 1,3,6,6-tetramethyifulvene in 10 mL of ether. The reaction mixture was allowed to warm to room temperature and stirred for 8 h! Successively, it was cooled to -30°C to add 3.13 mL of 1.6 M n-BuIi solution (5.0 mmol). The mixture was then allowed to warm to 0°C and treated with 1.16 g (5.0 mmol) of ZrCU. The reaction mixture was refluxed under stirring for 3 h and 10 mL of CH2CI2 was added at room temperature. The solution was isolated, concentrated and the residue was recrystallized from CEfeGa/hexane. Yield 0.58 g (23% based on 2,5-dimethyl-7H-cyclopenta[l^-b:43-b,]dithiophene). EXAMPLE 4 Synthesis of 2,2-(3-isopropyl-cyclopeiitadienyl)-7- dithiophene)propane 3.13 mL of a 1.6 M solution of n-BuLi (5 mmol) was added at -70°C to a solution of 1.03 g (5 mmol) of 2,5-dimethyl-7H-cyclopenta[l,2-b:4,3-b']-dithiophene in 20 mL of ether. The resulting mixture was stirred for additional 30 min at 0°C, then cooled again to -70°C and treated with 0.74 g (5 mmol) of 3-isopropyl-656-dimethylfulvene in 10 mL of ether. The reaction mixture was allowed to warm to room temperature and then treated with a saturated aqueous solution of NEUCl. The organic phase was isolated, dried by MgS04 and concentrated. The residue was recrystallized from hexane. Yield 0.85 g (48%). The title compound was characterized by *H-NMR spectroscopy. Synthesis of isopropy!idene{ (3-isopropyl-cyclopentadienyl)-7-(2,5-dimethyl-cyclopenta[l,2-b:4,3-b']-dithiophene) }zirconium dichloride C-2 3.75 mL of 1.6 M n-BuLi solution (6.0 mmol) was added at -70°C to a suspension of 1.06 g (3.0 mmol) of 2,2-(3-isopropyl^clopent^enyl)-7-(2,5Kiimetiiyl EXAMPLES Synthesis of 2£-(3-isopropyl-cyclopentadte^ [1,2- b;4?3-b,]-ditIiiophene)propaiie The same procedure as described in Example 4 for 2^2-(3-isopropyi-cyclopentadienyl)-7-(2,5- dimetliyl-(^clopenta[l,2-b:43-b^^ was followed excepting that 2,5- ditrimethylsilyl-7H-c^ (or 2,5-dimethyltrimertiiylsayl-7H- thienoP^^S^jcyclopent^bJthiophene) was used (see below). Synthesis of isopropylidene{ (S-isopropyl-cydopentadienyl^T^Z^S-ditrimethylsayl-cyciopenta[l^-b:43-b']-dithiophene) } zirconium dichloride C-7 3.05 mL of 1.6 M /i-BuLi solution (4.9 mmol) was added at -70°C to a solution of 1.57 g (4.86 mmol) of 2,5-ditrimetliylsilyl-7H-cyclopOT^ in 20 mL ether. The resulting mixture was stirred for additional 30 min at 0°C, then cooled again to -70°C and treated with 0.72 g (4.9 mmol) of 3-isopropyl-6,6-dimethylfulvene in 10 mL of ether. The reaction mixture was allowed to warm to room temperature and stirred for 4 It Successively, it was cooled to -30°C to add 3,05 mL of 1.6 M n-BuLi solution (4.9 mmol). The mixture was allowed to warm to 0°C and treated with 1.14 g (4.9 mmol) of ZrCl* The resulting reaction mixture was refluxed under stirring for 3 h, then the solution was isolated and concentrated. The residue was recrystallized from pentane. Yield 0.23 g (7.4% based on 2,5-ditrimeth3isilyl« TH-cyclopentafl^-b^jS-b'ldithiophene). The title compound was characterized by lH-NMR spectroscopy. EXAMPLE 6 Synthesis of 2^2-(3-i5opropyl-cyclopentadienyI)-4-(2?6-dimethyI-cycIopenta[25l-b:3,4- b']dithiophene)propane The same procedure as described in Example 4 was followed, excepting that 2,6-dimethyl-4H-cyclopenta[25l-b:3,4-b']dithiophene was used (see below). Synthesis of isopropylidene{ (3-isopropyl-cycIopentadienyI)-4-(256-dimethyl-cyclopenta[2,l-b:3,4-b']-dithiophene) } zirconium dichloride C-8 3.13 mL of 1.6 M n-BuLi solution (5.0 mmol) was added at-70 °C to a solution of 1.03 g (5.0 mmol) of 2,6-dimethyMH-cyclopenta[2,l-b:3,4-b']dithiophene in 20 mL of ether. The resulting mixture was stirred for additional 30 min at 0°C, then cooled again to -70°C and treated with 0.74 g (5.0 mmol) of 3-isopropyl-6,6-dimethylfulvene in 10 mL of ether. The mixture was allowed to warm to room temperature and stirred for 4 h. Successively, it was cooled to -30°C to add 3.13 mL of 1.6 M n-BuLi solution (5.0 mmol). The reaction mixture was allowed to warm to 0°C and treated with 1.16 g (5.0 mmol) of ZrCU- The resulting reaction mixture was refluxed under stirring for 3 h and subsequently 30 mL of CH2CI2 was added at room temperature. The solution was isolated and concentrated. The residue was recrystallized from CH2Cl2/hexane. Yield 0.87 g (34% based on 2,6-dimethyl-4H-cyclopenta[2,l-b:3,4-b']dithiophene). The title compound was characterized by 1H-!NMR spectroscopy. EXAMPLE 7 Synthesis of 2^3-tert-butyl-cyclopentadieEyI)-7-(2,S-dimethyl-cyclopenta [l,2-b:4,3-b']-dithiophene)propane 3.13 mL of a 1.6 M solution of n-BuLi (5 mmol) was added at -70°C to a solution of 1.03 g (5 mmol) of 2J5-dimethyi-7H-cyclopenta[l,2-b:4?3-b']-dithiophene in 20 mL of ether. The resulting mixture was stirred for additional 30 min at 0°C, then cooled again to -70°C and treated with 0.81 g (5 mmol) of S-tert-butyl-e^-dimethylfulvene in 10 mL of ether. The reaction mixture was allowed to wann to room temperature and then treated with a saturated aqueous solution of NH4CI. The organic phase was isolated, dried by MgS04 and concentrated. The residue was recrystallized from hexane. Yield 0.94 g (51%). The title compound was characterized by lH-NMR spectroscopy. Synthesis of isopropylidene{ (3-tert-buty^yclopentadienyl)-7--(295-diinet)iyl-cyclopenta[l^-b:43-b']-dithiophene) } zirconium dichloride C-3 3.75 mL of 1.6 M n-BuLi solution (6.0 mmol) was added at -70°C to a suspension of LI 1 g (3.0 mmol) of 2;2-(3-tert-butyl-cyclopen^ dithiophene)propane in 20 mL of ether. The mixture was allowed to warm to 0°C and treated with 0.7 g (3.0 mmol) of ZrCLj. The reaction mixture was refluxed under stirring for 3 h, then the yellow precipitate was filtered, washed twice with ether, dried and finally recrystallized from CH2C12. Yield 1.27 g (80%). The title compound was characterized by !H-NMR spectroscopy. EXAMPLE 8 Synthesis of 2^-{3-isopropyl-cyclopentadienyI)-7-(cyclopenta {l,2-*b:4,3-b']- dithiophene)propane 3.13 mL of 1.6 M solution of n-BuLi (5 mmol) was added to a solution of 0.89 g (5 mmol) of 7H-cyclopenta[l,2-b:4,3-b']dithiophene in 20 mL of THF at -70°C. The resulting mixture was stirred for additional 30 min at 0°C, then cooled again to -70°C and treated with 0.74 g (5 mmol) of 3-isopropyl-6,6-dimethjdfulvene in 10 mL of ether. The reaction mixture was allowed to warm to room temperature and then treated with a saturated aqueous solution of NH4CI. The organic phase was isolated, dried by MgS04 and concentrated. The residue was passed through a column packed with silica gel using hexane as eluent (Rf = 0.8). Yield 1.05 g (64%). The title compound was characterized by lH-NMR spectroscopy. Synthesis of isopropylidene(3-isopropyl-cyclopentadieuyI)-7-(cyclopenta[l?2-b:43-b']-dithiophene) zirconium dichloride C-16 A solution of 1.05 g (3.22 mmol) of 2,2-(3-isopropyl-cyclopentadienyl)-7-(cyclopenta [1,2- b:4,3-b']-dithiophene)propane in a mixture of 10 mL of ether and 60 mL of hexane was treated at -70°C with 4.1 mL (6.6 mmol) of a 1.6 M n-BuLi solution- The mixture was allowed to wann to 0°C and treated with 0.75 g (3.2 mmol) of ZrCU. The resulting reaction mixture was refluxed under stirring for 3 h, then the yellow precipitate was filtered, washed twice with hexane, dried and finally recrystallized from CBbCVhexane. Yield 0.32 g (21%), The title compound was characterized by lH-NMR spectroscopy. EXAMPLE 9 Synthesis of isopropylidene{(cyclopentadienyl)-7-(cyclopenta[l?2-b:4r3-b']- dithiophene)}zirconium dichloride C-0 It was carried out as described in the Example 6 of WO 98/22486. EXAMPLE 10 Synthesis of chloro(l-indenyI)dimethylsilane 37.5 mL of a 2.5 M solution of n-Buli in hexane (93.75 mmol, n-BuLi:indene = 1.1:1) was added dropwise to a solution of indene (purity 90 %, 11 g, 85.23 mmol) in 60 mL of Et2 hexane (40 mL) and added to a stirred solution of Me2SiCl2 (15.5 mL, 127.84 mmol, Me2SiCl2/IndLi = 1.5:1) in 50 mL of hexane, previously cooled to -78 °C. At the end of the addition, the mixture was allowed to reach room temperature and stirred overnight The suspension was then filtered, and the filtrate brought to dryness in vacuum to yield a pale yellow oil (16.5 g) of (l-Ind)SiMe2Cl free from its vinylic isomer (yield 89 %). !H NMR (D in ppm, CDC13): 021 (s, 3H, Si-CH3), 0.26 (s, 3H, Si-CH3), 3.77 (bs, 1H, Cp-H), 6.68 (dd, 1H, Cp-H), 7.03 (dd, 1H, Cp-H), 7.19-7.36 (m, 2H, Ar), 7.48-7.52 (m, 1H, Ar), 7.57-7.61 (m, 1H, Ar). Synthesis of (l-mdenyI)-7-(2,5-dimethyl-^cto^ dimethylsilane A 2.5 M solution of n-BuLi in hexane (4.80 mL, 12.00 mmol) was added at -20°C to a suspension of 2.25 g of 2,5-dimethyl-7H-cycIopen1a[l,2-b:4,3-b']Hdithiophene (Mw = 206.32, 10.90 mmol, w-BuLi: MeTh2Cp = 1.1:1) in 50 mL of ether. The resulting mixture was stirred for additional 1 h at 0°C with final formation of a dark brown suspension. This suspension was cooled again to -20°C and added of a solution of 2.20 g of chloro(l-indenyl)dimethylsilane(Mw = 208.76,10.54mmol,iodSiMe2ClMeTh2Cp= 1:1)in lOmLof ether. The reaction mixture was then allowed to warm to room temperature and stirred for 2 h. The final dark suspension (almost black) was concentrated under vacuum and the residue was extracted with 50 mL of toluene. The extract was dried under vacuum to give 4.06 g of a brown product, which was characterized by !H-NMR spectroscopy. The lH-NMR analysis showed the presence of the desired ligand (78.5wt%) together with 15.1wt% of starting IndSiMe2Cl and 6.4wt% of toluene. The ligand was used as such in the next step without further purification. Yield of the pure product = 79.9%. !H NMR (5, ppm, CDC13): -039 (s, 3H, Si-CH3); - 0.20 (s, 3H, Si-CH3); 2.57 (s, 6H, CH3); 3.82 (t, 1H, CH, J = 1.85 Hz); 3.89 (s, 1H, CH); 6.45 (dd, 1H, CH, J = 5.33 Hz, J = 1.85 Hz); 6.77-7.52 (m, 7H, Ar). Synthesis of dimethybity!{(l-tadeny^^ ditfaiophene)} zirconium dichloride C-10 A 2,5 M solution of «-BuLi in hexane (9.00 mL, 22.50 mmol) was added at -20°C to a solution of 4.06 g of (l-indenyl)-7 A 2.5 M w-BuLi solution in hexane (22.1 mL, 55.25 mmol, n-BuLi:2-Me-indene = 1.1:1) was added dropwise to a solution of 6,54 g of 2-methylindene (Boulder Scientific Company 419-0128, MW = 130.19, 50.23 mmol) in 70 mL of Et20, previously cooled to -20°C. At the end of the addition, the mixture was kept at -20°C for 15 min, then allowed to warm to room temperature and stirred overnight The solvents were evaporated off under reduced pressure to give a pale orange solid, which was taken up in 50 mL of hexane; the suspension was stirred for 10 minutes at room temperature and filtered. The lithium salt of 2-methylindene on the filter was washed with hexane (2 x 10 mL) and dried. The solid was again slurried in 70 mL of hexane and added to a stirred solution of Jd^SiCk (9.1 mL, d = 1.064, MW = 129.06, 75.02 mmol, Me2SiCl2/2-Me-IndIi = 1.5:1) in 60 mL of hexane, previously cooled to Q20°C. At the end of the addition, the pale orange slurry was kept at -20°C for 15 nun, then allowed to warm to room temperature and stirred overnight. The final white-pale yellow suspension was filtered and the filtrate brought to dryness in vacuo at 40°C to yield a yellow-orange oil as product (8.40 g). Yield = 75.1%. Purity = 89.1%. TH NMR (8, ppm, CDC13): 0.22 (s, 3H, Si-CH3), 0.47 (s, 3H, Si-CH3), 2.36 (m, 3H, CH3), 3.65 (bs, 1H, CH), 6.70 (m, 1H, Cp-H), 7.18-7.56 (m, 4H, Ar). About 6% (by GC-MS) of bis(2-methyl-l-indenyl)dimethylsilane (rac/meso = 1.3:1) was also present. m/z (%): 224 (28) [M* + 2], 222 (74) [M*], 129 (20), 128 (67), 127 (17), 95 (35), 93 (100). Alternative process without 2-Me-l-IndXi+ salt isolation A 25 M n-BuLi solution in hexane (23.6 mL, 59.00 mmol, «-BuLi:2-Me-indene * 1:1) was added dropwise to a solution of 7.87 g of 2-methylindene (Boulder Scientific Company 419-0128, MW = 130.19,97.6%, 59.00 mmol) in 50 mL of Et20, previously cooled to 0°C. At the end of the addition, the mixture was kept at 0°C for 15 min, then allowed to warm to room temperature and stirred for 2 h with final formation of a pale yellow suspension. It was cooled again to 0°C and added dropwise of Me2SiCl2 (7.86 mL, d - 1.064, MW *= 129.06, 64.80 mmol, Me2SiCl2/2-Me-IndLi = 1.1:1). At the end of the addition, the reaction mixture was allowed to warm to room temperature and stirred overnight. The final white-pale yellow suspension was concentrated in vacuo and the residue extracted with 30 mL of toluene. The extract was brought to dryness in vacuo at 40°C to yield a orange oil as product (10.41 g). Yield = 79.2%. Purity = 83.6%. Traces of starting 2-methylindene and 9.8% of bis(2-methyl-l-indenyi)dimethylsilane (by GC- MS) were also present. m/z for bis(2-methyl-l-indenyl)dimethylsaane (%): 316 (21) [M4], 187 (100\ 159 (24), 128 (18), 59 (57). Synthesis of (2-methyH-indenyI)-7-(2^-dimethyI-cyclopenta[l^-b:4>3-b,]-dithiophene) dimethylsilane A 2,5 M solution of w-BuLi in hexane (4.15 mL, 10.37 mmol) was added at -20°C to a solution of 2.13 g of 2,5-dimethyl-7H-cyclopenta[l^-b:4,3-b']-dithiophene (Mw » 206.32, 87.9% by GC-MS, 9.07 mmol, n-BuLi: MeTh2Cp = 1.1:1) in 20 mL of ether. The resulting mixture was stirred for additional 1 h at 0°C with final formation of a dark brown solution. This solution was cooled again to -20°C and added of a solution of 2.03 g of chloro(2-methyI-l-indenyl)dimethylsilane 9.10 mmol, (2-Me-l-Ind)SiM^Cl:MeTh2Cp = 1:1) in 3 mL of ether. The reaction mixture was then allowed to warm to room temperature and stirred for 2 h. The final dark solution (almost black) was concentrated under vacuum and the sticky residue was extracted with 50 mL of toluene. The extract was dried under vacuum to give 3.93 g of a brown sticky product, which was characterized by GC-MS analysis and !H-NMR spectroscopy. The ^-NMR analysis showed the presence of the desired ligand together with 10wt% of toluene. Purity (by GC-MS) = 90.4%. Yield of the pure product = 89.9%. *H NMR (5, ppm, CDC13): - 0.37 (s, 6H, Si-CH3); 2.26 (d, 3H, CH3, J = 0.8 Hz); 2.56 (dd, 3H, CH3, J - 1.1 Hz, J = 0.6 Hz ); 2.58 (dd, 3H, CH3, J = 1.1 Hz, J = 0.6 Hz); 3.88 (bs, 1H, CH); 4.04 (s, 1H, CH); 6.65-6.66 (m, 1H, CH); 6.87 (q, 1H, CH, J = 1.1 Hz); 6.89 (q, 1H, CH, J = 1.1 Hz); 7.10-7.50 (m,4H,Ar). m/z (%): 393 (13) [M* + 1], 392 (40) [M+], 263 (100), 235 (18), 187 (44), 159 (15), 59 (13). Synthesis of dimethylsilyl{ (2-methyl-l-indenyI)-7- A 2.5 M solution of «-BuLi in hexane (7.20 mL, 18.00 mmol) was added at -20°C to a solution of 3.93 g of (2-methyl-l-mdmyl)-7 diflriophene)dimethylsilane (Mw = 392.66, 90.4% by GC-MS, 8.15 mmol, 7i-BuIi:ligand = 2:1 considering the ligand 90.4% pure) in 30 mL of ether. The resulting mixture was stirred for additional 1 h at 0°C and 30 min at room temperature with final formation of a dark brown suspension. This suspension was cooled again at -20°C and added of a suspension of 1.91 g of ZrCU (Mw « 233.03, 8.20 mmol, ZrCU:ligand = 1:1 considering the ligand 90.4% pure) in 50 mL of pentane, previously cooled to -20°C. The reaction mixture was kept at -20°C for 1 h, then allowed to warm to room temperature and stirred overnight The final orange-pale brown suspension was evaporated off under vacuum and the residue washed with ether to give an orange powder (5.32 g), which was analysed by 5H-NMR in CD2CI2. The ^-NMR analysis showed the presence of the desired catalyst together with an adduct of coordination not identified (probably ZrCU(Et20)2 or UClfJEizO)). The powder was washed very quickly with 15 mL of HC14N9 then with water (30 mL), subsequently with EtOH (20 mL) and finally with Et20. After drying 3.50 g of pure catalyst as orange powder was recovered. Yield of the pure product =* 77.7%. . XH NMR (5, ppm, CD2C12): 1.20 (s, 3H, Si-CH3); 1.35 (s, 3H, Si-CH3); 2.39 (d, 3H, CK3, J = 0.59); 2.45 (d, 3H, CH3, J - 1.2 Hz); 2.62 (d, 3H, CH3, J - 1.2 Hz); 6.66 (q, 1H, CH, J = 1.2 Hz); 6.81 (bs, 1H, CH); 6.87 (ddd, 1H, CH, J - 0.98 Hz, J = 6.65 Hz, J = 9.0 Hz); 7.21 (ddd, 1H, CH, J == 0.98 Hz, J - 6.65 Hz, J - 8.61 Hz); 7.45 (dt, 1H, CH, J- 0.98, Hz J= 8.61 Hz); 7.73 (dq, 1H, CH, J = 0.98 Hz, J = 9.0 Hz). EXAMPLE 12 Synthesis of chloro(2-methyl-4-pheayl-l-indenyl)dimethylsilane A 2.5 M solution of n-BuLi in hexane (4.85 mL, 12.12 mmol) was added at 0°C to a solution of 2.50 g of 2-methyl-4-phenyl-indene (Boulder Scientific Company, Mw = 20629, 12.12 mmol, n-BuIi:2-Me-4~Ph-Ind = 1:1)in 30 mL of ether. The resulting mixture was stirred for additional 2 h at room temperature with final formation of an orange solution. This solution was cooled again to 0°C and added slowly of a solution of 1.58 mL of dichlorodimethylsilane (Aldrich, Mw = 129.06, d = 1.064,13.03 mmol, Me2SiCl2:2-Me-4-Pfa-Ihd = 1.08:1) in 20 mL of ether. The reaction mixture was then allowed to warm to room temperature and stirred for 1 h. The final straw yellow suspension was concentrated under vacuum and the residue was extracted with 50 mL of toluene. The extract was dried under vacuum to give 3.36 g of a straw yellow solid, which was characterized by GC-MS analysis and ^-NMR spectroscopy. Yield = 92.8%. lH NMR (8, ppm, CDC13): 0.24 (s, 3H, S1-CH3); 0.48 (s, 3H, Si-CH3); 2.31 (d, 3H, CH3, J - 0.78 Hz); 3.70 (bs, 1H, CH); 6.85 (m, 1H, CH, J - 0.78 Hz); 7.19-7.59 (m, 8H, Ar). m/z (%): 300 (26) [M* + 2], 299 (18) [M* + 1], 298 (72) [M*], 205 (23), 204 (45), 203 (28), 202 (32), 189 (15), 165 (13), 95 (35), 93 (100). Synthesis of (2-methyl-4-phenyI-l-indenyl)-7-(2?5-dimethyl-cyclopenta[l)2-b:4^-b']- dithiophene)dimethylsilane A 2.5 M solution of 72-BuLi in hexane (2.72 mL, 6-80 mmol) was added at -20°C to a solution of 1.40 g of 2,5-dimethyl-7H-cyclopenta[U-b:4,3-b']-dithiophene (Mw = 206.32, 90.7%, 6.15 mmol, w-BuLirMeTT^Cp = 1.1:1) in 30 mL of ether. The resulting mixture was stirred for additional 1 h at 0°C with final formation of a dark brown suspension. This suspension was cooled again to -20°C and added slowly of a solution of 1.90 g of chloro(2-methyl-4-phenyl- l-indenyi)dimethylsilane (Mw = 298.89, 6.37 mmol, (2-Me-4-Ph-l-Ind)SiMe2ClA4eTh2Cp = 1.04:1) in 20 mL of ether. The reaction mixture was then allowed to warm to room temperature and stirred for 2 h. The final dark solution (almost black) was concentrated under vacuum and the residue extracted with 50 mL of toluene to give an oily product, which was treated at 30°C under stirring with 30 mL of pentane. After 15 rnin stirring a powdery solid was formed and isolated by filtration. After drying in vacuo, 2.03 g of a brown product was recovered. Purity (by GC-MS) = 83.8%. Yield of the pure product = 59.0%. !H NMR (5, ppm, CDC13): - 0.35 (s, 3H, Si-CH3); - 0.32 (s, 3H, Si-CH3); 2.23 (d, 3H, CH3, J = 0.78 Hz); 2.55 (bs, 3H, CH3); 2.58 (bs, 3H, CH3); 3.96 (s, 1H, CH); 4.04 (s, 1H, CH); 6.82 (q, 1H, CH, J = 0.78 Hz); 6.86 (q, 1H, CH, J = 1.17 Hz); 6.88 (q, 1H, CH, J = 1.17 Hz); 7.13- 7.59 (m, 8H, Ar). m/z (%): 469 (10) [M+ + 1], 468 (24) [M*], 264 (28), 263 (100), 248 (14), 247 (21), 235 (20), 205 (13), 203 (16), 190 (10), 59 (14). Synthesis of dimethylsilyl{(2-methyM«phenyI-l-indenyI)-7-(2^dimethyl-cycIopenta[l)2- b:4^-b']-dithiophene)} zirconium dichloride C-28 A solution of 2.58 g (5.5 mmol) of (2-methyl-4-phenyl-l-indenyl)-7-(2»5-dimethyl-cyclopenta[l^-b:4,3-b']-difliiophene)dimetliylsilane in 40 mL of ether was treated at -70°C with 7.0 mL of a 1.6 M n-BuIi solution (11.2 mmol). The reaction mixture was allowed to Teach room temperature and stirred for 1 h. The solvent was removed under reduced pressure and the dilithium salt obtained was suspended in hexane. After cooling to -70°C, 1.28 g (5.5 mmol) of ZrCU were added. The reaction mixture was stirred at room temperature overnight, the yellow precipitate was filtered, washed twice with ether, dried and finally recrystallized from CH2CI2. Yield 1,65 g (48%). The title compound was characterized by XH NMR spectroscopy. EXAMPLE 13 Synthesis of (2-methyI-l-indenyQ-7-(cyclopenta[l^-b:4,3-b9]-dithiophene) dimethylsilane A 2.5 M solution of n-BuLi in hexane (1.50 mL, 3.75 mmol) was added at -20°C to a solution of 1.29 g of 7H-cyclopenta[l,2-b:4,3-b']-dithiophene (Mw = 178.28, purity valued by *H NMR ca. 50wt%, 3.62 mmol, n-BuLi:Th2Cp = 1.04:1) in 20 mL of ether. The resulting mixture was stirred for additional 1 h at 0°C with final formation of a dark brown suspension. This suspension was cooled again to -20°C and added of a solution of 0.96 g of chloro(2-methyH-indenyl)dimethylsilane (83,6% by GC-MS, Mw = 222.79, 3.62 mmol, (2-Me-l-Lad)S£Me2Q:Th2Cp = 1:1) in 5 mL of ether. The reaction mixture was then allowed to warm to room temperature and stirred for 2 h. The final black suspension was concentrated under vacuum and the sticky residue was extracted with 30 mL of toluene to remove the LiCl formed. The extract was dried under vacuum to give 2.26 g of a black oil, which was analysed by ^-NMR spectroscopy. Starting chIoro(2-metiiyl-l-indenyl)dimethylsilane, hexaethyisiloxane coming from previous steps and tars were also present as by-products, but attempts to purify the desired ligand failed because of the high solubility of the mixture in apolar solvent as pcntane. The crude product was then used as such in the next step without further purification. lH NMR (5, ppm, CDC13): - 0.36 (s, 3H, Si-CH3); - 0.35 (s, 3H, Si-CH3); 2.26 (d, 3H, CH3, J = 0.98 Hz); 3.89 (s, 1H, CH); 4.15 (s, 1H, CH); 6.69-7.52 (m, 9H, Ar). Synthesis of dtaethybflyl{(2-roeft^^ dithiophene)} zirconium dichloride C-36 A 23 M solution of »-BuLi in hexane (5.00 mL, 1250 mmol) was added at -20°C to a solution of 2.26 g of (2-methyl4-indenyl>7-(cyclopenta[lr2-b:43-b,3-didriophene)dimetiiylsilane (Mw * 364.61, 620 mmol, n-BuIi:ligand = 2.02:1 considering the ligand 100% pure) in 20 mL of ether. The resulting mixture was stirred for additional 1 h at 0°C with final formation" of a brown suspension. This suspension was cooled again to -20°C and added of a suspension of 1.44 g of ZrCU (Mw - 233.03, 6.20 mmol, ZrCl^ligand -1:1 considering the ligand 100% pure) in 30 mL of pentane, previously cooled to -20°C. The reaction mixture was kept at -20°C for 1 h, then allowed to warm up slowly to room temperature and stirred for 3 h. The final brown suspension was evaporated off tinder vacuum and the residue extracted with 30 mL of toluene: the extract, containing mainly tars, was eliminated, while the brown residue (3.33 g) was dried and washed with 20 mL of ether. The lH-NMR analysis in CD2CI2 showed for the residue from ether the presence of the desired catalyst together with an adduct of coordination not identified (probably ZiCUCE&O^ or LiCl(Et20)) and few tars. Again the brown powder (2.28 g) was washed very quickly with 20 mL of CH2CI2, then with EtOH (10 mL) and finally wife Et20 (15 mL). After drying 0.44 g of catalyst as pale brown powder was recovered. Yield ~ 13.5%. *H NMR (5, ppm, CEbCk): 1.25 (s, 3H, Si-CH3); 1.41 (s, 3H, Si-CH3); 2.38 (bs, 3H, CH3); 6.82-7.79 (m, 9H, Ar). EXAMPLE 14 A solution of 0.96 g (5.0 mmol) of 2-phenylindene in 30 mL of Et20 was treated at -70°C with 3.13 mL (5.0 mmol) of a 1.6 M solution of n-BuLi. After the addition, the mixture was allowed to warm to room temperature and stirred for 50 min. Then it was cooled again to - 70°C and treated with a solution of 0.65 g (5.0 mmol) of Me2SiCl2 in 10 mL of ether. When the addition was completed, the mixture was allowed to reach room temperature and stirred overnight The resulting reaction mixture was filtered to remove LiCl and the solvent was removed under reduced pressure. The crude product was used in the next step without further purification. 'H-NMR (8, ppm, C£)6): 7.90-7.10 (m, 9H, CH); 6.95 (s, 1H, CH); 4.15 (s, 1H, CH); -O.02 (s, 3H, Si-CH3); -0.20 (s, 3H, Si-CH3). Synthesis of dmeffiyfaflyl{(2-pbenyl-l-mdeny^ dithiophene)} zirconium dichloride C-31 A suspension of 1.03 g (5.0 mmol) of 2,5-dimethyl-7H-cyclopenta[l,2-b:4,3-b']-dithiophene in 30 mL of ether was treated at -70°C with 3.13 mL of a 1.6 M w-BuLi solution (5.0 mmol). After the addition, the resulting mixture was allowed to warm to room temperature and stirred for additional 50 min at this temperature. Then it was cooled again to -70°C and added of an efheral solution (10 mL) of chlorodimethyl-(2»phenyI-l-indenyi)silane coming from the previous step. The mixture was allowed to warm to room temperature and stirred overnight The ligand (2-phenyl-l-indenyl)-7-{(2,5-dimethyl^}^lopenta[l,2-b:4,3-b']- dithiophene)}dimethylsilane was characterized by lH-NMR spectroscopy. !H-NMR (6, ppm, CDC13): 7.70-7.25 (m, 9H, CH); 7.20 (s, 1H, CH); 6.90 (m, 2H, CH); 4.60 (s, 1H, CH); 3.70 (s, 1H, CH); 2.65 (s, 3H, CH3); 2.60 (s, 3H, CH3); -0.44 (s, 3H, Si-CH3); -0.66 (s, 3H, Si-CH3). The ligand was not isolated: its solution was treated at -70°C with 7.0 mL of a 1.6 M n-Buli solution (11.2 mmol). Then the reaction mixture was allowed to reach room temperature and stirred for 1 b. The solvent was removed under reduced pressure and the dilithium salt obtained was suspended in hexane. After cooling to -70oC, 1.28 g (5.5 mmol) of ZrCU were added. The reaction mixture was stirred at room temperature overnight, the red precipitate was filtered, washed twice with ether, dried and finally recrystallized from CH2CI2. Yield 1.64 g (53% based onMe2Th). EXAMPLE 15 Synthesis of (2-methyl-l-indeny^-7- dithiophene)dimethylsilane A suspension of 1.17 g (5.0 mmol) of 2,5-die1hyl-7H-cyclopenta[l,2-b:4,3-b']-dithiophene in 75 mL of ether was treated at -70°C with 3.13 mL of a 1.6 M n-Buli solution (5.0 mmol). After the addition, the mixture was allowed to warm to room temperature and stiired for additional 1 h at this temperature. Then it was cooled again to -70°C and added of a solution of 1.11 g (5 mmol) of chloro(2-methyi-l-indenyl)dimethylsilane in 10 mL of ether. The resulting mixture was allowed to reach room temperature and stiired overnight The ligand (2- me&yl-l-mdenyl)-7-(2,5-diethyl^ was not isolated, but used in solution for the catalysts synthesis (see below). 'H-NMR (5, ppm, CDC13): 7.55 (d, 1H, CH); 7.44 (d, 1H, CH); 7.28 (m, 1H, CH); 7.15 (m, 1H, CH); 6.98 (m, 1H, CH); 6S6 (m, 1H, CH); 6.70 (m, 1H, CH); 4.10 (s, 1H, CH); 3.94 (s, 1H, CH); 2.98 (m, 4H, CH2); 2.31 (s, 3H, CH3); 1.43 (t, 3H, CH3); 1.41 (t, 3H, CH3); -0.30 (s, 3H, S1-CH3); -0.31 (ss 3H, S1-CH3). Synthesis of dimethylsilyl{(2-methyM dithiophene)} zirconium dichloride C-34 The ligand solution coming from the previous step was treated at -70°C with 7.0 mL of a 1.6 M n-BuLi solution (11.2 mmol). Then the reaction mixture was allowed to reach room temperature and stirred for 1 h. The solvent was removed under reduced pressure and the dilithium salt so-obtained was suspended in hexane. After cooling to -70°C, 0.75 g (3.2 mmol) of ZrCU were added. The reaction mixture was stirred at room temperature overnight, the yellowish-red precipitate was filtered, washed twice with ether, dried and finally recrystallized from CH2CI2. Yield 1.52 g (52% with respect to Et2Th). EXAMPLE 16 Synthesis of (2-methyl-l-indenyl)-7- dithiophene)dimethylsilane A solution of 1.32 g (4.0 mmol) of 2,5-diphenyl-7H-cyclopenta[l,2-b:4,3-b']-dithiophene in 30 mL of ether was treated at -70°C with 2.50 mL of a 1.6 M w-BuIi solution (4.0 mmol). After the addition, the mixture was allowed to warm to room temperature and stirred for additional 50 min at this temperature. Then it was cooled again to -70°C and added of a solution of 0.90 g (4.0 mmol) of chlorodimethyl(2-methyl-l-indenyl)silane in 10 mL of ether. The resulting mixture was allowed to reach room temperature and stirred ovemightThe ligand (2-methyl- l-indenyl)-7*(2,5-diphenyl-cyclopenta[ 1 ,2-b:4,3-b5]-dithiophene)dimethylsilane was not isolated, but used in solution for the catalysts synthesis. Synthesis of dimethylsilyl{ (2-methy^l-indenyI)-7-(2,5-dipheny^cyclopenta[l^-b:4^-b,]-dithiophene)} zirconium dichloride C-35 The ligand solution coming from the previous step was treated at -70°C with 5.6 mL of a 1.6 M 7z-BuIi solution (9.0 mmol). Then the reaction mixture was allowed to reach room temperature and stirred for additional 1 h. After cooling to -70°C, 1.05 g (4.5 mmol) of ZrCU were added. The reaction mixture was stirred at room temperature overnight, then the violet precipitate was filtered, washed twice with ether, dried and finally recrystallized from CH2CI2. Yield 1.27 g (47% with respect to Ph2Th). EXAMPLE 17 Synthesis of 3,6,6-trimethylfulvene A solution of 2-methyl-l,3-cyclopentadiene (125 g, 1.56 mol) in 12 L of ethanol was treated at low temperature with 126 mL (1.72 mol) of acetone and 142 mL (1.72 mol) of pyrrolidine. The resulting solution was kept below room temperature overnight Then the reaction mixture was neutralized with a 10 % aq. solution of H3PO4, extracted with hexane (3 x 150 mL) and washed with water until neutral pH. The organic phase was separated, dried with MgSC>4 and concentrated The residue was distilled at 70°C/60mmHg. Yield 112.6 g (60%). *H NMR (8, ppm, CDCI3): 6.53 (dd, 1H, CH); 6.35 (dd, 1H, CH); 6.20 (m, 1H, CH); 2.17 (s, 3H, CH3); 2.16 (s, 3H, CH3); 2.09 (s, 3H, CH3). Synthesis of 3-isopropyl-l-methyl-l,3-cyclopentadiene A solution of 24 g (02 mol) of 3,6,6-trimethylfulvene in 100 mL of ether was added at -78°C under argon atmosphere to a solution of 7.59 g (0.2 mol) of lithium aluminium hydride in 200 mL of ether. The reaction mixture was allowed to warm to room temperature, stirred for 2 h and then treated with a 10% aq. solution of NH4CI. The organic phase was collected, washed with water, dried with MgSCU and concentrated. The residue was distilled at 63°C/50 mmHg. Yield 15.88 g (65%).The desired title compound was characterized by 'H-NMR. Synthesis of l-methyl-3-isopropyl-6?6-dimetbylfu]vene 3-isopropyl-lmethyH3-cyclopentadiene (39 g, 0.32 mol) was added at low temperature to a suspension of 12.8 g (0.32 mol) of sodium hydroxide in 200 mL of dry THR After 30 min stirring, the reaction mixture was treated with 23.8 mL (0.32 mol) of acetone. The resulting solution was kept below room temperature overnight. Then the resulting mixture was neutralized with a 10 % aq. solution of H3PO4, extracted with hexane (3 x 100 mL) and washed with water until neutral pH. The organic phase was separated, dried with MgSCU and concentrated. The residue was distilled at 80°C/10mmHg. Yield 25.96 g (50%). 'H NMR (5, ppm, CDCI3): 6.21 (m, 1H, CH); 6.05 (d, 1H, CH); 2.67 (m, 1H, CH); 224 (s, 3H, CH3); 2.21 (s, 3H, CH3); 2.20 (s, 3H, CH3); 1.26 (s, 3H, CH3); 1.28 (s, 3H, CH3). Synthesis of 2^2HmethyI^isopropyI^clopentadi^^ b:43-b'] dithiophene)propane A 1.6 M solution of n-BuLi (6.25 mL, 10 mmol) was added at -70°C to a suspension of 2.06 g (10 mmol) of 2,5-dimethyl-7H-cyclopenta[l,2-b:4,3-b']-dithiophene in 100 mL of ether. At the end of the addition, the mixture was allowed to warm to room temperature and stirred for additional 50 min at the same temperature. The resulting reaction mixture was treated at -70°C with a solution of 0.74 g (5 mmol) of l-methyl-3-isopropyl-6,6-dimethylfulvene, then was allowed to warm to room temperature and stirred overnight The final mixture was poured into 100 mL of a 10% aq. solution of NH4CI and extracted with hexane (2 x 50 mL). The organic phase was collected, washed with water, dried with MgS04 and evaporated off. The residue was passed through a column packed with Si02 by using hexane as eluent The resulting solution was dried giving the crystalline product Yield 1.5 g (41% based on starting MeTh2Cp). Synthesis of isopropflydene^(2-methyl^isopropylH^clopentadienyl)-7K2^Hiimethyl- cydopenta[l,2-b:43-b']-dithiophene) ^zirconium dichloride C-17 A suspension of 1.11 g (3 mmol) of 2,2^2-methyl^isopropyl-l-cyclopentadienyl)-7-"{ (2,5- dimethylKyclopenta[l,2-b:43"b']dithiophene)lpropane in 10 mL of ether and 50 mL of hexane was treated at -70°C with 3.8 mL of a 1.6 M n-BuIi solution (6.1 mmol). After the addition, the reaction mixture was allowed to warm to 0°C and added of 0.75 g (3.2 mmol) of ZrCU- The resulting mixture was allowed to reach room temperature and sthred overnight Then the yellow precipitate obtained was filtered, washed twice with ether, dried and finally recrystallyzed from CH2CI2. Yield 1.43 g (90%). ]H-NMR (8, ppm, CD2C12): 6.88 (m, 1H, CH); 6.80 (m, 1H, CH); 6.10 (d, 1H, CH); 5.58 (d, 1H, CH); 2.78 (m, 1H, CH); 2.58 (m, 3H, CH3); 2.56 (d, 3H, CH3); 2.40 (s, 3H, CH3); 2.18 (s, 3H, CH3); 1.96 (s, 3H, CH3); 1.14 (d, 3H, CH3); 1.08 (d, 3H, CH3). EXAMPLE 18 Synthesis of l^-dimethyl-l^-cyclopentadiene A solution of 25 g (0.26 mol) of 3-methyl-2-cyclopenten-l-one in 100 mL of ether was added at -78°C under argon atmosphere to a solution of methyl litium in 200 mL of ether, previous prepared from 5.76 g (0.83 mol) of lithium and 26 mL (0.42 mol) of iodomefhane. The reaction mixture was stiired for 4 h and then treated with a 10% aq. solution of NH4CL The organic phase was collected, washed with water, dried with MgS04 and concentrated. The residue was distilled at 42°C/100 mmHg. Yield 13 g (30%). 'H-NMR (5, ppm, CD3COCD3): 5.98 (m, 1H, CH); 5.75 (m, 1H, CH); 2.80 (m, 2H, CH2); 2.02 (d, 3H, CH3); 1.90 (d, 3H, CH3). The ligand synthesis was carried out by coupling the lithium salt of the MeTt^Cp precursor with cMoro(294-dimethylcyclopentadienyl)dimethylsilane, previous prepared from the lithium salt of l,3-dimethyM,3-cyclopentadiene and MeaSiCb. Synthesis of dimethylsilyll (2,4-dimethyl-cydopentadieny^7K2^-dimethyl-cydopenta[l^ b:43-b']-dithiophene) ^zirconium dichloride C-18 A suspension of 1.07 g (3 mmol) of (2,4-dimeliiyI 70°C with. 4.1 mL of a 1.6 M n-BuLi solution (6.5 mmol). After the addition, the reaction mixture was allowed to warm to 0°C and added of 0.75 g (3.2 mmol) of ZrCL*. The resulting mixture was allowed to reach room temperature and stirred overnight Then the yellow precipitate obtained was filtered, washed twice with ether, dried and finally recrystallyzed from CH2C12. Yield 1.35 g (87%). ]H-NMR (8, ppm, CD2C12): 6.93 (m, 1H, CH); 6.87 (m, 1H, CH); 6.80-6.70 (m, 1H, CH); 6.25 (t, 1H, CH); 2.59 (d, 3H, CH3); 2.56 (d, 3H, CH3); 2.18 (s, 3H, CH3); 2.11 (s, 3H, CH3); 1.03 (s, 3H, Si-CH3); 0.84 (s, 3H, Si-CH3). EXAMPLE 19 Synthesis of dimethylsflyli(3-tert-butyI-cyclopentadienyI>-7 b:4r3-b']-dithiophene)l'zirconium dichloride C-4 The synthesis was carried out by following the same procedure described in the Example 18 by using 3-tert-butyl-l,3-cyclopentadiene instead of l,3-dimethyl-l,3-cyclopentadiene. The product was characterized by NMR spectroscopy. EXAMPLE 20 Synthesis of isopropilydenei (tetramethyl-cydopentadienyI)-7-(2,5-dimethyl- cyclopenta[l,2-b:4,3-b']-ditluophene) ^zirconium dichloride C-5 The synthesis was carried out by following the same procedure described in the Example 17 by using 1^,3,4,6,6-esamethylfolvene instead of l-methyl-3-isopropyl-6,6-dimethylfulvene. The product was characterized by NMR spectroscopy. EXAMPLE 21 Synthesis of dimethylsilyl^ (3-trimethyIsflyI-^clopentadienyI>7-(2?5-dimetiiyl- cyclopenta[1^4>:4,3-b*]-dithiophene)i> The ligand synthesis was carried out by coupling the lithium salt of the MeTt^Cp precursor with chloro(3-1rimethylsilyl^yclopentadienyl)dimethylsilane, previous prepared from the lithium salt of trimethylsilyl-l,3-cyclopentadiene and M^SiCfe. Synthesis of dimefliylsiIyl^(3-trimethylsflyl-cydopentad]eny^7^2^dimetty]- cyclopenta[l?2-b;4,3-b,]-dithiophene)hzirconiuni dichloride C-9 A suspension of 1.20 g (3 mmol) of (3-trimethylsilyl-l-cyclopentadienyl)-7^(2,5-dimethjd- cyclopenta[l,2-b:4,3-bJ]dithiophene)l>dimethylsilane in 20 mL of ether was treated at -70°C with 4.1 mL of a 1.6 M n-BuLi solution (6.5 mmol). After the addition, the reaction mixture was allowed to warm to 0°C and added of 0.75 g (3.2 mmol) of ZrCU. The resulting mixture was allowed to reach room temperature and stirred overnight Then the yellow precipitate obtained was filtered, washed twice with ether, dried and finally recrystallyzed from CH2CI2- Yieldl.l7g(70%). lH-NMR (8, ppm, CD2C12): 6.91 (m, 1H, CH); 6.88 (m, 1H, CH); 6.78 (m, 1H, CH); 6.08 (t, 1H, CH); 5.83 (t, 1H, CH); 2.59 (d, 3H, CH3); 2.57 (d,3H, CH3); 0.91 (s, 3H, Si-CH3); 0.89 (s, 3H, Si-CH3); 0.20 (s, 9H, Si(CH3)3). EXAMPLE 22 Synthesis of l-methy!-3-phenyH»3-cyclopentadiene A solution of 25 g (0.26 mol) of 3-methyl-2-cyclopenten-l-one in 100 mL of ether was added at -78°C under argon atmosphere to a solution of phenyl litium in 200 mL of ether, previous prepared from 5.76 g (0.83 mol) of lithium and 44 mL (0.42 mol) of bromobenzene. The reaction mixture was stirred for 4 h and then treated with a 10% aq. solution of NH4CI. The organic phase was collected, washed with water, dried with MgS04 and concentrated The residue was distilled at 54°C/1 mmHg. Yield 2437 g (60%). ^-NMR (5, ppm, CD3COCD3): 7.60-7.10 (m, 5H, CH); 6.80 (d, 1H, CH); 6.00 (m, 1H, CH); 3.00 (s, 2H, CH2); 1.98 (q, 3H, CH3). Synthesis of l-methyI-3-phenyl-6,6-dimethylfalvene A solution of l-methyl-3-phenyH,3-cyclopentadiene (15.62 g, 0.1 mol) in 100 mL of ethanol was treated at low temperature with 8.6 mL (0.12 mol) of acetone and 9.7 mL (0.12 mol) of pyrrolidine. The resulting solution was kept below room temperature overnight Then the reaction mixture was neutralized with a 10 % aq. solution of H3PO4, extracted with hexane (3 x 50 mL) and washed with water until neutral pH. The organic phase was separated, dried with MgS04 and concentrated. The residue was distilled at 85°C/10mmHg. Yield 5.89 g (30%). The desired title compound was characterized by ^-NMEL The ligand synthesis was carried out by following the same procedure described in the Example 17, by using l-methyl-3«phenyl-6,6-dimethylfiilvene instead of l-methyl-3- isopropyl-6,6-dimethylfialvene * and 2,5^trimethylsilyl-7H-cyclopenta[l^-b:4,3- b*]dithiophene instead of MeTT^Cp. Synthesis of isopropilydend (2-methyl-4-phenyl-cyclopentadienyI)-7-(2?5- trimethylsDylcyclopenta [l?2-b:43-b,]-dithiophene)hdrconium dichloride C-14 A suspension of 2.0 g (3.85 mmol) of 2^-(2-methyl-4-phenyl-l-cyclopentadien5d)»7-(2,5-trimethylsilylcyclopenta[l:2-b:4,3-bJ]-dithiophene)propane in 50 mL of ether was treated at -70°C with 4.8 mL of a 1.6 M' n-BuLi solution (7.71 mmol). After the addition, the reaction mixture was allowed to warm to 0°C and added of 0.90 g (3.85 mmol) of ZrCU- The resulting mixture was allowed to reach room temperature and stirred overnight Then the brown precipitate obtained was filtered, washed twice with ether, dried and finally recrystallyzed from CH2CI2. Yield 1.82 g (70%). 2H-NMR (8, ppm, CD2C12): 7.34 (s, 2H, CH); 7.32-7.12 (m, 5H, CH); 6.62 (d, 1H, CH); 6.26 (d, 1H, CH); 2.50 (s, 3H, CH3); 2.30 (s, 3H, CH3); 2.10 (s, 3H, CH3); 0.36 (s, 9H, Si(CH3)3); 0.32 (s, 9H, Si(CH3)3). EXAMPLE 23 Synthesis of isopropilydene*!(2-methyl-4-phenyl-cyclopentadienyl)- 7-(2,5-dimetfiy]r cyclopenta[l^-b:4^-b']-ditiuophene)fzircoiiinm dichloride C-ll The synthesis was carried out by following the same procedure described in the Example 22 by using 2,5-dimethyl-cyclopenta[l^-b:4,3-b,]-dithiophene instead of 2,5-trimethylsilylcyclopenta [l,2-b:4,3-V]-difhiophene. The product was characterized by NMR. spectroscopy. EXAMPLE 24 Synthesis of isopropflydene,{(4-phenyl-cyclopentadienyl)- 7-(2,5-dimethyI-cyclopenta[l?2-b:43-b']-dithiophene)}^irconium dichloride C-19 The synthesis was carried out by following the same procedure described in the Example 22 by using 3-phenyl-6,6-dimethyifulvene instead of l-methyl-3-phenyl-696-dimethylfidvene. The product was characterized by NMR spectroscopy. EXAMPLE 25 The synthesis of l,3-dimethyl-l,3-cyclopentadiene has been reported above in the Example 18. Synthesis of 1,3,6,6-tetramethylfulvene A solution of l,3-dimethyl-l,3-cyclopentadiene (9.42 g, 0.1 mol) in 100 mL of ethanol was treated at low temperature with 8.6 mL (0.12 mol) of acetone and 9.7 mL (0.12 mol) of pyrrolidine. The resulting solution was kept below room temperature overnight. Then the reaction mixture was neutralized with a 10 % aq. solution of H3PO4, extracted with hexane (3 x 50 mL) and washed with water until neutral pH. The organic phase was separated, dried over MgS04 and concentrated. The residue was distilled at 63°C/20mmHg. Yield 6.7 g (50%). *H NMR (8, ppm, CDC13): 6.08 (m, 1H, CH); 6.03 (m, 1H, CH); 2.23 (d, 3H, CH3); 2.17 (s, 3H, CH3); 2.16 (s, 3H, CH3); 1.99 (s, 3H, CH3). The ligand synthesis was carried out by following the same procedure described in the Example 17, by using 1,3,6,6-tetramethylfolvene instead of l-methyl-3-isopropyI-6,6- dimethyifulvene and 2s5-ditrimelliylsilyl-7H-^clopenta[l^-b:4,3-b']dithiophene instead of MeTh2Cp. Synthesis of isopropilydene*i(2,4-dimethyI-cyclopentadienyl)-7-(2,5- trimethylsilylcyclopenta[l,2-b:4,3-b']-dithiophene) Zirconium dichloride C-15 A suspension of 2.19 g (4.8 mmol) of 2,2-(2,4-dimethyl-l-cyclopentadienyl)-7-(2,5-trimethylsilylcyclopenta[1^2-b:4,3-b,]-dithiophene)propane in 50 mL of ether was treated at -70°C with 6.0 mL of a 1.6 M n-BuLi solution (9.6 mmol). After the addition, the reaction mixture was allowed to warm to 0°C and added of 1.12 g (4.8 mmol) of ZrCU. The resulting mixture was allowed to reach room temperature and stirred overnight. Then the red-brown precipitate obtained was filtered, washed twice with ether, dried and finally recrystallyzed from CH2CI2. Yield 2.07 g (70%). The desired title compound was characterized by ^-NMR. EXAMPLE 26 Synthesis of 3-chloro-2-methyI-2-butenal 1.3 mol (120 mL) of POCI3 was added at 0°C to a 1.6 mol (120 mL) of DMF. At the end of the addition, the mixture was allowed to warm to room temperature and stirred for 1 h. Then it was cooled again to 0°C and treated with 1 mol (90 mL) of 2-butanone. The resulting reaction mixture was allowed to reach room temperature and stirred overnight Then it was poured into a mixture of ice and water, added of sodium acetate and extracted with CHCI3 (3 x 150 mL). The organic phase was separated, washed with water "until neutral pH, dried over MgS04 and evaporated off to dryness. The residue was distilled in vacuo, b.p. 45°C/10 torr. Yield 73 g (62%). Synthesis of 4^-dimethyl-2-thiophene-etliylcarboxylate Ethyl-2-mercaptoacetate (0.2 mol, 24 g) was added at 0°C to a solution of sodium ethoxide (021 mol, 14.3 g) in 150 mL of ethanol and the resulting mixture was stirred at the same temperature for 30 min. Then 3-chloro-2-methyl-2-butenal (0.2 mol, 23.7g) was added and stirring was continued overnight. The resulting product was diluted in 100 mL of water, the organic layer was collected and the water layer was extracted with CH2CI2 (2 x 150 mL). The combined organic layers were dried over MgSO^ evaporated off to dryness and the residue distilled in vacuo. Yield 22.48 g (61%). 'H-NMR (8, ppm, CDCU): 7.52 (s, 1H, CH); 4.32 (q, 2H, OCH2); 2.35 (s, 3H, CH3); 2.12 (s, 3H, OH3); 135 (t, 3a CH3). Synthesis of 4^-dimethyI-2-thiophenecarboxyIic acid 4,5-dimethyl-2-tinophene»ethylcarboxylate (0.122 mol, 22.48 g) was added to a 30% solution of sodium hydroxide in 100 mL of ethanol and the resulting mixture was refluxed for 2 h. Thai it was diluted in water, acidified and filtered. The precipitate was dried under P2O5. Yield 15.6 g (82%). !H-NMR (8, ppm, CDCI3): 7.60 (s, 1H, CH); 2.42 (s, 3H, CH3); 2,17 (s, 3H, CH3). Synthesis of 23-dhnethylthiophene The 4J5-dimethyl-2-thiophenecarboxyiic acid prepared as described above (0.58 mo!, 90 g) was heated to 180°C until the evolution of carbon dioxide ceased- The product was collected and distilled, b.p. 140°C. Yield 30 g (46%). !H-NMR (5, ppm, CDC13): 7.02 (d, 1H, CH); 6.82 (d, 1H, CH); 2.42 (s, 3H, CH3); 220 (s, 3H, CH3)- Synthesis of 2^^trimethyl-5)6-dihydro-4H-*cyclopenta[b]thiophene-4-one A solution of 10 g of P2O5 (0.07 mol) in 100 mL of methanesulfonic acid (1.54 mol) was heated at 80°C under stirring. A mixture of 2,3-dimethtylthiophene (0.27 mol, 30 g) and methacryiic acid (0.35 mol) in 20 mL of CH2CI2 was added and the resulting reaction mixture was stirred at the same temperature for 1.5 h. Then it was poured into a mixture of ice and water and stirred vigorously. The water layer was extracted with CH2CI2 (3 x 50 mL), the organic layers were collected, washed with a 10% aqueous solution of sodium carbonate until neutral pH and finally with water. Then the organic phase was isolated, dried over MgS04, evaporated off to dryness and distilled in vacuo, b.p. 110°C/1 torr. Yield 10 g (20%). ^-NMR (5, ppm, CDCI3): 3.35 (dd, 1H, CH2); 2.98 (qd, 1H, CH); 2.66 (dd, 1H, CH2); 2.35 (s, 3H, CH3); 2.25 (s, 3H, CH3); 1.52 (d, 3H, CH3). Synthesis of 293?5-trunethyl-6H-cyclopenta[b]thiophene (or 2,3^-trimethyH-thiopentalene) A solution of 2,3,5-trimethyl-5,6-dihydro»4H-c^clopentaIT)]thiophene-4-one (11 g, 61 mmol) in 100 mL of ether was slowly added to a solution of LiAJH4 (1.16 g, 30 mmol) in 100 mL of ether and stirred overnight. The resulting suspension was poured into a mixture of ice and water, the organic layer was isolated, while the water layer was extracted with ether (3 x 50 mL). The combined organic layers were washed with water, dried over MgS04 and evaporated off to dryness. The 2,3,54rimethyl-5,6-dihydro^H^yclopento^ so • obtained was dissolved in 100 mL of benzene, added of 1 g ofp-toluenesulfonic acid and was refluxed for 10 mm. Then the reaction mixture was cooled to room temperature and treated with a saturated aqueous solution of Na2C03- The organic phase was isolated, dried over MgSCU and evaporated off to dryness. Yield 8 g (80% based on starting ketone). 'H-NMR (8, ppm, CDC13): 6.44 (m, 1H, CH); 3.05 (s, 2H, CH2); 2.45 (s, 3H, CH3); 2.20 (s, 3H, CH3); 2.15 (s, 3H, CH3). Synthesis of 6H-6-(2,3^-trimethyl-cyclopenta[b]thiophene)chlorodimethylsilane A solution of 1.28 g (5 mmol) of 2,3,5-trimethyl-6//: Synthesis of dimethylsilyl{ 6-(2,3^-trimethyl-cyclopenta[b]thiophene)-7-(23-dimethyl-cyclopenta[l^-b:43-b']-dithiophene)} zirconium dichloride C-27 A suspension of 0.9 g (4.4 mmol) of 2,5-dimeth}d-7^cyclopen.ta[l^-b:43-b']-ditbiophene in 20 mL of ether was treated at »70°C with 2.75 mL of a 1.6 M n-BuIi solution (4.4 mmol). 4 After the addition, the resulting mixture was allowed to warm to room temperature and stirred for additional 50 mm at this temperature. Then it was cooled again to -70°C and added of an etheral solution (10 mL) of 6H-6-(2,3,5-trimethyl- cyclopenta[b]thiophene)chlorodime&ylsilane coming from the previous step. The mixture was allowed to warm to room temperature and stirred overnight The ligand 6-{(23s5-trme%i-cycto^ b']dithiophene)}dimethylsilane so-obtained was characterized by *H-NMR. !H-NMR (5, ppm, C&e): 6 JO (m, 2H, CH); 6.50 (s, 1H, CH); 4.40 (s, 1H, CH); 4.10 (s, 1H, CH); 2.39 (m, 3H, CH3); 2.37 (d, 6H, CH3); 2.25 (s, 3H, CH3); 2.14 (s, 3H, CH3); 0.18 (s, 3H, Si-CH3); 0.07 (s, 3H, Si-CH3). The ligand was not isolated: its solution was treated at-70°C with 5.60 mL of a 1.6 M «-BuIi solution (9.0 mmol). Then the reaction mixture was allowed to reach room temperature and stirred for 1 h. The solvent was removed under reduced pressure and the dilithium salt obtained was suspended in hexane. After cooling to -70°C, 1.17 g (5 mmol) of ZrCU were added. The reaction mixture was stirred at room temperature overnight, the yellow precipitate was filtered, washed twice with ether, dried and finally recrystallized from CH2CI2. Yield L62 g (60% with respect to Me2Th). The desired title compound was characterized by^H-NMR spectroscopy. EXAMPLE 27 Synthesis of 3-chloro-2-methyl-3-phenyl-2-propenal 1.2 mol (110 mL) of POCI3 was added at 0°C to a 2.8 mol (216 mL) of DMF (excess of DMF used as solvent). At the end of the addition, the mixture was allowed to warm to room temperature and stirred for 1 h. Then it was cooled again to 0°C and treated with 1 mol (134 g) of piopiophenone. The resulting reaction mixture was allowed to reach room temperature and stirred overnight Then it was poured into a mixture of ice and water, added of sodium acetate and extracted with CHCI3 (3 x 150 mL). The organic phase was separated, washed with water until neutral pH, dried over MgS04 and evaporated off to dryness. The residue was distilled in vacuo, ixp. 120°C/10toir. Yield 163 g (90%). !H-NMR (8, ppm, CDCI3): 9.52 (s, 1H, CHO); 7.45 (m, 5H, CH); 2.12 (s, 3H, CH3). Synthesis of 4-methyl-5-phenyl-2-tliiophene-ethylcarboxylate Ethyl-2-mercaptoacetafce (0.9 mol, 100 mL) was added at 0°C to a solution of sodium ethoxide (1 mol, 68 g) in 500 mL of ethanol and the resulting mixture was stirred at the same temperature for 30 min. Then 3-chloro-2«methyl-3-phenyl-2-propenal (0.9 mol, 163 g) was added and stirring was continued overnight. The resulting product was diluted in 1.5 L of water, the organic layer was collected and the water layer was extracted with CH2CI2 (4 x 150 mL). The combined organic layers were dried over MgSC>4, evaporated off to dryness and the residue was used in the next step without further purification. The title compound was characterized by lH-NMR spectroscopy. Synthesis of 4-methyl-5-phenyI-2-thiophenecarboxyIic acid The 4-methyl-5-phenyl-2-thiophene-ethylcarboxylate coming from the previous step was added to a 30% solution of sodium hydroxide in 1 L of ethanol and the resulting mixture was refiuxed for 2 h. Then it was diluted in water and extracted with 200 mL of benzene. The water phase was isolated, acidified and the mixture was filtered. The precipitate was dried under P2O5. Yield 127 g (65% with respect to 03-chloro-2-methyl-3-phenyl-2«propenal). 'H-NMR (5, ppm, CDCI3): 7.75 (s, 1H, CH); 7.50^7.40 (m, 5H, CH); 237 (s, 3H, CH3). Synthesis of 3-methyl-2-phenylthiophene The 4-methyl-5«phenyi-2-thiophenecarboxylic acid (127 g, 0.58 mol) prepared as described above was heated to 220-230°C until the evolution of carbon dioxide ceased. The product was collected and distilled, b.p. 120°C/10 ton. Yield 30.3 g (30%). !H-NMR (8, ppm, CDC13): 7.60 (d, 2H, CH); 7.48 (t, 2H, CH); 7.35 (t, 1H, CH); 7.25 (d, 1H, CH); 6.98 (d, 1H, CH); 2.39 (s, 3H, CH3). Synthesis of 2-formyl-4-methyI-5-phenyIthiophene 0.35 mol (32 mL) of POCl3 was added at 0°C to a 1.0 mol (77 mL) of DMF (excess of DMF used as solvent). At the end of the addition, the mixture was allowed to warm to room temperature and stirred for 1 h. Then it was cooled again to 0°C and treated with 3-methyl-2-phenylthiophene (60 g, 0.35 mol). The resulting reaction mixture was allowed to reach room temperature and after 12 h stirring at the same temperature was heated at 80°C for 2 days. Then it was poured into a mixture of ice and water, added of sodium acetate and extracted with CHCI3 (3 x 150 mL). The organic phase was separated, washed with water until neutral pH, dried over MgSC>4 and evaporated off to dryness. The residue was crystallized. Yield 60.2 g (85%). lH-NMR (5, ppm, CDCI3): 9.88 (s, 1H, CHO); 7.62 (s, 1H, CH); 7.55-7.40 (m, 5H, CH); 2.39 (s, 3H, CH3). Synthesis of 2-methyI-3-(4-methyI-5-phenyl-2-thienyI)-acrjiic acid A mixture of 2-formyl-4-methyl^5-phenylthiophene (20.2 g, 0.1 mol) and ethyl-2-bromopropionate (0.12 mol, 15.5 mL) was added to a suspension of Zn (7 g, 0.1 mol) in 150 mL of benzene with a catalytic amount of HgBr2. The resulting mixture was refluxed under stirring while all amount of Zn will not be dissolved, and subsequently dissolved in water. The organic layer was isolated, washed with a 10% aq. solution of HC1, dried over MgSC>4 and evaporated off to dryness. The residue, corresponding to 2-methyl-3-(4-methyl-5-phenyl-2- thienyl)ethyl acrylate, was used without further purification in the synthesis of the related acid. In fact, it was added to a 30% aq. solution of sodium hydroxide in 100 mL of ethanol and refluxed for 2 h. The resulting reaction mixture was diluted in water, acidified and filtered. The precipitate was dried under P2O5. Yield 16.7 g (65%). *H-NMR (5, ppm, CDCI3): 7.90 (s, 1H, CH); 7.50-7.30 (m, 5H, CH); 7.20 (s, 1H, CH); 2.40 (s, 3H, CH3); 220 (s, 3H, CH3). Synthesis of 2-methyl-3-(4-methyl-5-phenyl-2-thienyI)-2-propanoic acid The desired 2«methyl-3-(4-methyl-5-phenyl-2-thienyl)-2-propanoic acid was obtained by electrochemical reduction of 2-methyl-3-(4-methyl-5-phenyl-2-thienyl)acrylic acid. Yield *100%. ^-NMR (5, ppm, CDCI3): 7.50-7.30 (m, 5H, CH); 6.70 (s, 1H, CH); 3.30 (dd, 1H, CH); 2.90 (m, 2H, CH2); 230 (s, 3H, CH3); 1.30 (d, 3H, CH3). Synthesis of 3^dimethyI-2-phenyl-556-dihydro-4H-cyclopenta[b]thiophene-4-one A solution of 3 g of P2O5 (21 mmol) in 30 mL of methanesulfonic acid (0.46 mol) was heated at 80°C under stirring. A solution of 2-methyl-3-(4-methyl-5-phenyl-2-thienyl)-2-propanoic acid (65 mmol, 16.9 g) in 20 mL of CH2CI2 was added' and the resulting reaction mixture was stirred at the same temperature for 1.5 h. Then it was poured into a mixture of ice and water and stirred vigorously. The water layer was extracted with CH2CI2 (3 x 50 mL), the organic layers were collected, washed with a 10% aqueous solution of sodium carbonate until neutral pH and finally with water. Then the organic phase was isolated, dried over MgS04 and evaporated off to dryness. Yield 6.3 g (40%). !H-NMR (6, ppm, CDC13): 7.50-7.40 (m, 5H, CH); 3.40 (dd, 1H, CH2); 3.05 (m, 1H, CH); 2.80 (dd, 1H, CH2); 2.55 (s, 3H, CH3); 1.40 (d, 3H, CH3). Synthesis of 3^-dimethyI-2-phenyl-6H-^ycIopenta[b]thiophene (or 3?5-dimethyl-2-phenyl-1-thiopentalene) A solution of 3,5-dimethyl-2-phenyi-5,6-dihydro^H-^^ (6.3 g, 26 mmol) in 75 mL of ether was slowly added to a solution of liAJHt (0.5 g, 13 mmol) in 50 mL of ether and stirred overnight The resulting suspension was poured into a mixture of ice and water, the organic layer was isolated, while the water layer was extracted with ether (3 x 50 mL). The combined organic layers were washed with water, dried over MgSC>4 and evaporated off to dryness. The 3,5-^Imethyl-2-phenyl-5,6-dihydro^ so obtained was dissolved in 100 mL of benzene, added of 1 g ofp-toluenesulfonic acid and was refluxed for 10 min. Then the reaction mixture was cooled to room temperature and treated with a saturated aqueous solution of Na2C03. The organic phase was isolated, dried over MgSC>4 and evaporated off to dryness. Yield 4.66 g (80% based on the starting ketone). 'H-NMR (8, ppm, CDC13): 7.50-7.40 (m, 5H, CH); 6.50 (q, 1H, CH); 3.20 (d, 1H, CH2); 2.60 (dd, 1H, CH2); 2.20 (s, 3H, CH3); 1.66 (s, 3H, CH3). Synthesis of 6H-6-(2-phenyI-3j5-dimethyl-cyclopenta[b]thiophene)chloro dimethylsilane A solution of 1.70 g (7.5 mmol) of 3,5-dimefh)i-2-phenyl-6i?-cyclopenta[b]thioph9ne in 40 mL of Et20 was treated at -70°C with 5.0 mL (8 mmol) of a l;6 M solution of n-BuLi. After the addition, the mixture was allowed to warm to room temperature and stored for 1 h. Then it was cooled again to -70°C and treated with a solution of 1.30 g (10 mmol) of Me2SiCl2 in 10 mL of ether. When the addition was completed, the mixture was allowed to reach room temperature and stirred overnight. The resulting reaction mixture was filtered to remove IiCl and solvent was removed under reduced pressure. The crude product was used as such in the next step without further purification. !H-NMR (5, ppm, C£>6): 7.60-7.20 (m, 5H, CH); 6.50 (m, 1H, CH); 3.40 (s,1H, CH); 2.84 (s, 3H, CH3); 221 (s, 3H, CH3); 0.39 (s, 3H, Si-CH3); 0.12 (s, 3H, Si-CH3). Synthesis of dimethyMyI{6^2-phenyI-3,5-dimethyI-c^^ dimethyl-cydopenta[l^-b:4^-b']-dithiophene)} zirconium dichloride C-29 A suspension of 1.3 g (6.3 mmol) of 2,5-dime&yl-7H-^clopen1a[l^ in 30 mL of ether was treated at -70°C with 4.0 mL of a 1.6 M n-BuIi solution (6.4 mmol). After the addition, the resulting mixture was allowed to warm to room temperature and stirred for additional 50 min at this temperature. Then it was cooled again to -70°C and added of an etheral solution (10 mL) of 6H-6-(3,5-dimethyl-2-phenyl- cyclopenta[b]thiophene)chlorodimethylsilane coming from the previous step. The mixture was allowed to warm to room temperature and stirred overnight The ligand 6-{(3,5-dimethyl-2- phenyl- cyclopenta[b]thiophene)} -7- {(2,5-dimethyl-cyclopenta[l ,2-b:4,3-b' ]- dithiophene)}dimethylsilane so-obtained was characterized by ^-NMR. *H-NMR (8, ppm, C6D6): 7.60-7.10 (m, 5H, CH); 6.85 (s, 1H, CH); 6.80 (s, 1H, CH); 6.-50 (m, 1H, CH); 4.37 (s, 1H, CH); 4.10 (s, 1H, CH); 2.38 (d, 3H, CH3); 2.37 (d, 3H, CH3); 236 (s, 3H, CH3); 2.12 (s, 3H, CH3); -0,05 (s, 3H, Si-CH3); -0.16 (s, 3H, Si-CH3). The ligand was not isolated: its solution was treated at -70°C with 8.2 mL of a 1.6 M n-Buli solution (13.1 mmol). Then the reaction mixture was allowed to reach room temperature and stirred for 1 h. The solvent was removed under reduced pressure and the dilithium salt obtained was suspended in hexane. After cooling to -70°C, 1.51 g (6.5 mmol) of ZrCU were added. The reaction mixture was stirred at room temperature overnight, the yellow-brown precipitate was filtered, washed twice with ether, dried and finally recrystallized from CH2CI2. Yield 2.30 g (56% with respect to Me2Th). The desired title compound was characterized by * 'H-MMR. JH-NMR (5, ppm, CD2C12): 7.44-7.36 (m, 5H, CIO; 6.86 (q, 1H, CH, J = 124 Hz); 6.73 (q, 1H, CH, J = 1.24 Hz); 6.56 (bs, 1H, CH); 2.63 (d, 1H, CH3, J - 124 Hz); 2.50 (d, 3H, CH3, J = 1.24 Hz); 2.35 (s, 3H, CH3); 2.20 (s, 3H, CH3); 1.22 (s, 3H, Si-CH3); 1.14 (s, 3H, Si-CHs). EXAMPLE 28 Synthesis of 3-chloro-2,3-diphenyl-2-propenal 0.25 mol (23 mL) of POCl3 was added at 0°C to a 0.3 mol (23.5 mL) of DMF. At the end of the addition, the mixture was allowed to waim to room temperature and stirred for 1 h. Then it was cooled again to 0°C and treated with 0.1 mol (19.6 g) of deoxybenzoin. The resulting reaction mixture was allowed to reach room temperature, stirred for 12 h at the same temperature and subsequently heated at 100°C for 2 h. Finally it was poured into a mixture of ice and 10% solution of sodium acetate in water* The oily precipitate was filtered and washed with cold methanol and hexane. The residue was crystallized. Yield 18.5 g (76%). XH-NMR(8, ppm, CDC13): 9.70 (s, 1H, CHO); 7.60-7.20 (m, 10H, CH). Synthesis of 4j5-diphenyl-2-thiophene-ethylcarboxylate Ethyl-2-mercaptoacetate (40 mmol, 4.4 mL) was added at 0°C to a solution of sodium ethoxide (42 mmol, 2.86 g) in 50 mL of ethanol and the resulting mixture was stirred at the same temperature for 30 min. Then 3-chloro-2,3-diphenyl-2-propenal (37 mmol, 9.0 g) was added and stirring was continued overnight The resulting orange suspension was heated at 50°C for 2 h, then cooled to room temperature and diluted in 100 mL of water. The so-obtained red solution containing a precipitate was extracted with Et20 (3 x 50 mL). The combined organic layers were washed with NHjCl/water, dried over MgSCU and evaporated off to dryness. The solid residue was recrystallized from hexane. Yield 9.2 g (81%). !H-NMR (8, ppm, CDC13): 7.40-7.30 (m511H, CH); 4.40 (q, 2H, CH2); 1-40 (t, 3H, CH3). Synthesis of 4,5-diphenyl-2-thiophenecarboxylic acid The 4,5-diphenyl-2-thiophene-ethylcarboxylate (3.6 g, 12 mmol) coming from the previous step was added to a 30% solution of sodium hydroxide in 20 mL of ethanol and the resulting mixture was refluxed for 2 h. Then it was diluted in water and the water phase was acidified. The white precipitate obtained was filtered and dried at 80°C, Yield 3.16 g (94%). lH-NMR (8, ppm, (CD3)2SO): 7.80 (s, 1H, CH); 7.40-7.30 (m, 10H, CH). Synthesis of 2,3-diphenylthiophene The 4,5-diphenyl-2-thiophenecarboxylic acid (28 g, 0.1 mol) prepared as described above was heated to 220-230°C until the evolution of carbon dioxide ceased. The residue was diluted ia water and extracted with 100 mL of benzene. The organic phase was dried over MgSCU and evaporated off to give the crystallized product. Yield 22.45 g (95%). XH-NMR (5, ppm, CDC13): 7.35 (d, 1H, CH); 7.34-7.26 (m, 10H, CH); 7.19 (d, 1H, CH). Synthesis of 2-formyI-4^-diphenyIthiophene POCl3 (80 mmol, 7.32 mL) was added at 0°C to a solution of 2,3-diphenylthiophene (18 g, 76 mmol) in DMF (18 mL, 0.23 mol). At the end of the addition, the reaction mixture was allowed to warm to room temperature and refluxed for 3 h. Then it was cooled to room temperature and poured into a mixture of ice and a 10% solution of sodium hydroxide in water. The oily precipitate obtained was filtered and washed with cold methanol and hexane. The residue was crystallized. Yield 15 g (75%). 'H-MMR (5, ppm, CDCI3): 9.95 (s, 1H, CHO); 7.82 (s, 1H, CH); 7.40-7.25 (m, 10H, CH). Synthesis of 2-methyl-3-(4^-diphenyl-2-thieny0-ethyl acrylate A mixture of 2-formyl-4,5-diphenylthiophene (14.8 g, 56 mmol) and ethyl-2-bromopropionate (60 mmol, 7.8 mL) was added to a suspension of Zn (4.25 g, 65 mmol) in 100 mL of benzene with a catalytic amount of I2. The resulting mixture was refluxed under stiiring while all amount of Zn will not be dissolved, and subsequently dissolved in water. The organic layer was isolated, washed with a 10% aq, solution of HG, dried over Mg304 and evaporated off to dryness. The residue was dissolved into 50 mL of benzene and was refluxed with 0.5 g of p-toluenesulfonic acid for 1 h. Then the reaction mixture was cooled to room temperature and treated with a saturated aqueous solution of Na^Qj. The organic phase was isolated, dried over MgSC>4 and evaporated off to dryness. Yield 17.6 g (90%). lH-NMR (8, ppm, CDCI3): 7.90 (s, 1H, CH); 7.40-7.25 (m, 11H, CH); 4.30 (q, 2H, CH2); 2.30 (d, 3H, CH3); 1.40 (t, 3H, CH3). Synthesis of 2-methyl-3-(4,5-diphenyI-2-thienyl)-acrylic acid The 2-methyl-3»(4,5-diphenyl-2-thienyl)-ethyl acrylate (18.9 g, 54 mmol), coming from the previous step, was added to a 30% aq. solution of sodium hydroxide in 300 mL of ethanol and refluxed for 2 1L The resulting reaction mixture was diluted in water, acidified and filtered. The precipitate was dried under P205. Yield 12.1 g (70%). 'H-NMR (8, ppm, (CD3)2SO): 7.85 (d, 1H, CH); 7-55 (s, 1H, CH); 7.40-7.20 (m, 10H, CH); 2.15(s,3H,CH3). Synthesis of 2-methyI-3-(4,5-diphenyI-2-thienyI)-2-propanoic acid The desired 2-methyl-3-(4,5-diphenyl-2-thienyl)-2-propanoic acid was obtained by electrochemical reduction of 2«metiiyl-3-(4J5-diphenyl-2-thienyl)-acrylic acid. Yield «100%. *H-NMR (8, ppm, (CD3)2SO): 7.30-7.15 (m, 10H, CH); 6.90 (s, 1H, CH); 3.10 (dd, 1H, CH); 2.70 (m, 2H, CH2); 1.10 (d, 3H, CH3). Synthesis of 5-methyI-2^-diphenyl-5?6-dihydro-4H-cyclopenta[b]thiopheiie-4-oiie A solution of P2O5 (2.6 g, 18 mmol) in 15 mL of methanesulfonic acid (0.23 mol) was heated at 80°C under stirring. A solution of 2-me1hyl-3-(4,5^phenyl-2-thienyi)-2-prppanoic acrid (18 mmol, 6.0 g) in 20 mL of CH2CI2 was added and the resulting reaction mixture was stirred at the same temperature for 15 min. Then it was poured into a mixture of ice and water and stirred vigorously. The water layer was extracted with CH2CI2 (3 x 50 mL), the organic layers were collected, washed with a 10% aqueous solution of sodium carbonate until neutral pH and finally with water. Then the organic phase was isolated, dried over MgSO* and evaporated off to dryness. The residue was passed through a column packed with silica gel 60 by using a mixture hexane/ethyl acetate = 5/1 as eluent The evaporation of the red fraction was given the crystallized product. Yield 2.18 g (40%). !H-NMR (8, ppm, CDC13): 7.40-7.20 (m, 10H, CH); 3.50 (dd, 1H, CH2); 3.05 (m, 1H, CH); 2.85 (dd, 1H, CH2); 1.40 (d, 3H, CH3). Synthesis of 5-dimethyl-2,3-diphenyl-6H-cyclopenta[b]thiophene (or 5-dimethyI-2,3-diphenyM-thiopentalene) A solution of 5-methyl-2,3^phenyI-5,6- JH-NMR (5, ppm, CDCI3): 7.40-7.20 (m, 10H, CH); 6.48 (q, 1H, CH); 3.24 (s, 2H, CH2); 2.24 (d, 3H, CH3). Synthesis of 6H-6-(5-methyl-2,3-diphenyl-cyclopenta[b]thiophene)chloro dimethylsilane A solution of 1.28 g (4.4 mmol) of 5-methyl-2^^phen>i-6if^clopenta[b]fhiophene in 40 mL of Et20 was treated at -70°C with 3.5 mL (5.6 mmol) of a 1.6 M solution of /z-BuLL After the addition, the mixture was allowed to warm to room temperature and stirred for 1 h. Then it was cooled again to -70°C and treated with a solution of 1.30 g (10 mmol) of Me2SiCl2 in 10 mL of ether. When the addition was completed, the mixture was allowed, to reach room temperature and stirred overnight. The resulting reaction mixture was filtered to remove IiCl and the solvent was removed under reduced pressure. The crude product was used as such in the next step without further purification. 'H-NMR (5, ppm, CeDe): 7.60-7.00 (m, 10H, CH); 6.56 (m, 1H, CH); 3.40 (s, 1H, CH); 2.13 (s, 3H, CH3); 0.37 (s, 3H, Si-CH3); 0.15 (s, 3H, S1-CH3). Synthesis of dimethyIsilyl{6-(5-methyl-2?3-dipheny]-cyclopenta[b]thiophene)-7-(2?5-dimethyt-cyclopenta[l^-b:4y3Mb']-dithiophene)} zirconium dichloride C-30 A suspension of 0.9 g (4.4 mmol) of 2,5-dimethyl-7H-cyclopenta[l92-b:4,3-b']-dithiophene in 30 mL of ether was treated at -70°C with 3.0 mL of a 1.6 M ?i-BuLi solution (4.8 mmol). After the addition, the resulting mixture was allowed to warm to room temperature and stirred for additional 50 min at this temperature. Then it was cooled again to -70°C and added of an etheral solution (10 mL) of 6H-6-(5-methyl-2,3-diphenyl- cyclopenta[b]thiophene)chlorodimethylsilane coming from the previous step. The mixture was allowed to warm to room temperature and stirred overnight The Iigand 6-{(5-me£byl-2,3- diphenyl-cyclopenta[>]tMop dithiophene)}dimethylsilane so-obtained was characterized by ^-NMR. !H-NMR (5, ppm, C£>6): 7.60-7.00 (m, 10H, CH); 6.85 (m, 1H, CH); 6.80 (m, 1H, CH); 6,60 (m, 1H, CH); 4.35 (s, 1H, CH); 4.10 (s, 1H, CH); 2.40 (d, 3H, CH3); 2.38 (d, 3H, CH3); 2.05 (s, 3H, CH3); 0.05 (s, 3H, Si-CH3); -0.20 (s, 3H, Si-CH3). The Iigand was not isolated: its solution was treated at -70°C with 5.6 mL of a 1.6 M n- BuLi solution (9.0 inmol). Then the reaction mixture was allowed to reach room temperature and stirred for 1 b. The solvent was removed under reduced pressure and the dilithium salt obtained was suspended in hexane. After cooling to ~70°C, 1.17 g (5.0 mmol) of ZrCU were added. The reaction mixture was stirred at room temperature overnight, the yellow precipitate was filtered, washed twice with ether, dried and finally recrystallized from CH2CI2. Yield 1.46 g (47% with respect to Me2Th), *H-NMR (5, ppm, CD2CI2): 7.39-7.24 (m, 10H, CH); 6.88 (q, 1H, CH, J - 1.17 Hz); 6.76 (q, 1H, CH, J = 1.17 Hz); 6.59 (bs, 1H, CH); 2.63 (d, 3H, CH3, J - 1.17 Hz); 2.51 (d, 3H, CH3> J = 1.17 Hz); 2.35 (s, 3H, CH3); 1.25 (s, 3H, S1-CH3); 1.16 (s, 3H, Si-CH3)- EXAMPLE 29 Synthesis of 3-chloro-2-phenyl-2-butenal CHO 0.375 mol (35 mL) of POCl3 was added at 0°C to a 0.45 mol (35 mL) of DMF. At the end of the addition, the mixture was allowed to warm to room temperature and stirred for 1 h. Then it was cooled again to 0°C and carefully treated with 0.15 mol (20.1 g) of phenylacetone. The resulting reaction mixture was stirred at the same temperature for 1 h. Then it was poured into a mixture of ice and water, added of sodium acetate and extracted with CHCI3 (3 x 50 mL). The organic phase was separated, washed with water until neutral pH, dried over MgS04 and carefully evaporated off to dryness. The residue was distilled in vacuo, b.p. 90-110°C/0.21 torr. Yield 10 g (37%). 'H-NMR (8, ppm, CDCI3): 10.50 (s, 1H, CHO); 7.40-7.00 (m, 5H, CH); 2.20 (s, 3H, CH3). Synthesis of 5-methyl-4-phenyl-2-thiophene-ethylcarboxylate Ethyl-2-mercaptoacetate (45.8 mmol, 5 mL) was added at 0°C to a solution of sodium efhoxide (46 mmol, 3.13 g) in 50 mL of ethanol and the resulting mixture was stirred at the same temperature for 30 min. Then 3-chloro-2-phenyl-2-butenal (45.8 mmol, 8.27 g) was added and stirring was continued overnight The resulting product was refluxed for 2 h, cooled to room temperature and diluted in 100 mL of water. The organic layer was collected and the water layer was extracted with CH2Q2 (3 x 50 mL). The combined organic layers were dried over MgS04» evaporated off to dryness and the residue was used in the next step without further purification. The title compound was characterized by TH-NMR spectroscopy. Synthesis of 5-methyI-4-phenyl-2-thiophenecarboxyIic acid The 5-methyI-4-phenyl-2-thiophene-ethylcarboxylate coming from the previous step was added to a 30% solution of sodium hydroxide in 100 mL of ethanol and the resulting mixture was refluxed for 2 h. Then it was diluted in water and extracted with 50 mL of benzene. The water phase was isolated, acidified and the mixture was filtered The precipitate was dried under P2O5. Yield 9.5 g (95% based on 3«chloro-2-phenyl-2-butenal). lH-NMR (6, ppm, CDCI3): 12.00 (s, 1H, COOH); 7.90 (s, 1H, CH); 7.50-7.40 (m, 5H, CH); 2.55 (s, 3H, CH3). Synthesis of 2-methyI-3-phenyIthiophene The 5-methyl-4-phen)4-2-thiophenecarboxylic acid (54 g, 0.25 mol) prepared as described above was heated to 220-230°C until the evolution of carbon dioxide ceased. The product was collected and distilled, b.p. 117°C/10 torr. Yield 30 g (70%). !H-NMR (5, ppm, CDC13): 7.45 (m, 5H, CH); 7.15 (d, 1H, CH); 7.10 (d, 1H, CH); 2.55 (s, 3H, CH3). Synthesis of 2-formyl-5-methyl-4-phenylthiophene 0.166 mol (15 mL) of POCi3 was added at 0°C to a 0.5 mol (39 mL) of DMF. At the end of the addition, the mixture was allowed to warm to room temperature and stirred for 1 h. Then it was cooled again to 0°C and treated with 2-methyl-3-phenyithiophene (29 g, 0.166 mol). The resulting reaction mixture was allowed to reach room temperature and after 12 h stirring at the same temperature was heated at 80°C for 2 days. Then it was poured into a mixture of ice and water and added of sodium acetate. The precipitate so obtained was filtered, washed with water and subsequently with hexane. The yellow powder was dried in vacuo. Yield 27.7 g (83%). ^-NMR (5, ppm, CDCI3): 9.88 (s, 1H, CHO); 7.70 (s, 1H, CH); 7.55-7.40 (m, 5H, CH); 2.55 (s, 3H, CH3). Synthesis of 2-methyl-3-(5-methyI-4-phenyl-2-thienyI)-ethyl acrylate A mixture of 2-form>1-5-methyl-4-phenylthiophene (27.6 g, 0.136 mol) and ethyl-2-bromopropionate (0.14 mol, 18.2 mL) was added to a suspension of Zn (9.8 g, 0.15 mol) in 250 mL of benzene with a catalytic amount of I2. The resulting mixture was refluxed under stirring while all amount of Zn will not be dissolved, and subsequently dissolved in water. The organic layer was isolated, washed with a 10% aq. solution of HC1, dried over MgSC>4 and evaporated off to dryness. The residue was used without further purification in the synthesis of the related acid. The title compound was characterized by ]H-NMR spectroscopy. Synthesis of 2-methyl-3-(5-methyI-4-phenyl-2-thienyI)-acrylic acid The 2-methyl-3-(5-methyl^phenyl-2-tbienyl)-ethyl acrylate coming from the previous step was added to a 30% aq. solution of sodium hydroxide in 200 mL of ethanol and refluxed for 2 h. The resulting reaction mixture was diluted in water, acidified and filtered. The precipitate was dried under P2O5. Yield 26.0 g (74% based on 2-fonnyl-5-methyl-4-phenyltiiiophene). lH-NMR (5, ppm, CDC13): 7.90 (s, 1H, CH); 7.50-7.30 (m, 5H, CH); 7.25 (d, 1H, CH); 2.60 (s, 3H, CH3); 2.25 (s, 3H, CH3). Synthesis of 2-methyl-3-(5-methyl-4-phenyl-2-thienyl)-2-propanoic acid The desired 2-methyl-3^5-methyl^phenyl-2-thienyl)-2-propanoic acid was obtained by electrochemical reduction of 2-methyl-3-(5-methyl«4-phenyl-2-thienyl)acrylic acid. Yield *100%. !H-NMR (5, ppm, CDC13): 7.50-7.20 (m, 5H, CH); 6.80 (s, 1H, CH); 3.25 (dd, 1H, CH); 2.85 (m, 2H, CH2); 2.50 (s, 3H, CH3); 1.30 (d, 3H, CH3). Synthesis of 2j5-dimethyl-3-phenyl-5,6-dihydro-4H-cycIopenta[b]thiophene-4-one A solution of 3 g of P2O5 (21 mmol) in 30 mL of methanesulfonic acid (0.46 raol) was heated at 80°C under stirring. A solution of 2-methyl-3-(5-methyl-4-phenyl-2-thienyl)-2-propanoic acid (65 mmol, 16.9 g) in 20 mL of CH2CI2 was added and the resulting reaction mixture was stirred at the same temperature for 1.5 k Then it was poured into a mixture of ice and water and stirred vigorously. The water layer was extracted with CH2CI2 (3 x 50 mL), the organic layers were collected, washed with a 10% aqueous solution of sodium carbonate until neutral pH and finally with water. Then the organic layers were collected, dried over MgS04 and evaporated off to dryness. The residue was passed through a column packed with silica gel 60 by using a mixture of hexane/ethyl acetate = 3/1 as eluent. The evaporation of the red fraction was given the oily product. Yield 4.4 g (28%). 'H-NMR (5, ppm, CDCI3): 7.50-7.40 (m, 5H, CH); 3.42 (dd, 1H, CH2); 3.02 (m, 1H, CH); 2.79 (dd, 1H, CH2); 2.50 (s, 3H, CH3); 1.35 (d, 3H, CH3). Synthesis of 2,5-dimethyl-3-"phenyl-6H-cyclopenta[b]thiophene (or 2,5-dimettiyl-3-phenyl-1-thiopentalene) A solution of 2,5-dimethyl-3^henyl-5,6-Ki^ (4.4 g, 18 mmol) ia 50 mL of ether was slowly added to a solution of LLAIH4 (035 g, 9 mmol) in 50 mL of ether and stirred overnight The resulting suspension was poured into a mixture of ice and water, the organic layer was isolated, while the water layer was extracted with ether (3 x 50 mL). The combined organic layers were washed with water, dried over MgS(>4 and evaporated off to dryness. The 2,5-dimethyl-3-phenyl-5,6-«iihydr^ 4~ol so obtained was dissolved in 100 mL of benzene, added of 1 g ofp-toluenesulfonic acid and was refluxed for 10 rain. Then the reaction mixture was cooled to room temperature and treated with a saturated aqueous solution of Na2CC>3. The organic phase was isolated, dried over MgS04 and evaporated off to dryness. The residue was passed through a column packed with AI2O3 by using hexane as eluent. The evaporation of the yellow fraction was given the crystallized product. Yield 1.5 g (37% based on the starting ketone). JH-NMR (8, ppm, CDCI3): 7.50-7.40 (m, 5H, CH); 6.52 (q, 1H, CH); 3.24 (d, 1H, CH2); 2.60 (d, 1H, CH2); 2.24 (dd, 3H, CH3); 1.66 (s, 3H, CH3). Synthesis of 6H-6-(2^-dimethyl-3-phenyl"Cyclopenta[b]thiophene)chloro dimethylsilane A solution of 120 g (5.3 mmol) of 2,5-dimethyl-3-phenyl-6^-cyclopenta[b]thiophene in 40 mL of Et20 was treated at-70°C with 3.3 mL (5.3 mmol) of a 1.6 M solution of n-BuLL After the addition, the mixture was allowed to warm to room temperature and stirred for 1 h. Subsequently it was cooled again to -70°C and treated with a solution of 1.30 g (10.1 mmol) of Me2SiCl2 in 10 mL of ether. When the addition was completed, the mixture was allowed to reach room temperature and stirred overnight. The resulting reaction mixture was filtered to remove LiCl and solvent was removed under reduced pressure. The crude product was used as such in the next step without further purification. !H-NMR (8, ppm, CeD6): 7.45-7.20 (m, 5H, CH); 6.50 (m, 1H, CH); 3.40 (s, 1H, CH); 2.38 (s, 3H, CH3); 2.12 (s, 3H, CH3); 036 (s, 3H, Si-CH3); 0.11 (s, 3H, Si-CH3). Synthesis of dimethylsiIyI{6^2,5-dimethyI-3-pheny]-cycIopenta[b]thiophene>7-(2,5-dimethyl-cyclopenta[l92-b:493-'b,]-ditliiopheiie)} zirconium dichloride C-33 A suspension of 0.9 g (4.4 mmol) of 2,5-dimethyl-7H-cyclopenta[l^»b:4,3-b']-dithiophene in 30 mL of ether was treated at -70°C with 3.0 mL of a 1.6 M n-BuIi solution (4.8 mmol). After the addition, the resulting mixture was allowed to warm to room temperature and stirred for additional 50 min at this temperature. Then it was cooled again to -70°C and added of an etheral solution (10 mL) of 6H-6-(2,5-dimethyl-3-phenyl- cyclopente(TD]thiophene)cHorodimethylsilane coming from the previous step. The mixture was allowed to warm to room temperature and stirred overnight. The ligand 6-{(2,5-dimethyl-3- phenyI !H-NMR (8, ppm, CDC13): 7.45-7.20 (m, 5H, CH); 6.85 (s, 1H, CH); 6.80 (s, 1H, CH); 6.60 (m, 1H, CH); 4.30 (s, 1H, CH); 4.00 (s, 1H, CH); 2.70 (d, 3H, CH3); 2.65 (d, 3H, CH3); 2.60 (s, 3H, CH3); 2.30 (s, 3H, CH3); -0.18 (s, 3H, Si-CH3); -0.30 (s, 3H, Si-CH3). The ligand was not isolated: its solution was treated at -70°C with 5.6 mL of a 1.6 M «- BuLi solution (9.0 mmol). Then the reaction mixture was allowed to reach room temperature and stirred for 1 h. The solvent was removed under reduced pressure and the dilithium salt obtained was suspended in hexane. After cooling to -70°C, 1.17 g (5.0 mmol) of ZrCU were added. The reaction mixture was stirred at room temperature overnight, the yellow precipitate was filtered, washed twice with ether, dried and finally recrystallized from CH2CI2. Yield 1.68 g (59% with respect to Me2Th). The desired title compound was characterized by lH-NMR spectroscopy. EXAMPLE 30 Synthesis of l-bromo-2-(3-indenyl)ethane A 1.6 M w-BuLi solution in hexane (100 mL, 0.16 mol) was added at 0°C to a solution of indene (18.6 g, MW - 116.16, 0.16 mol) in 300 mL of ether. The resulting suspension was allowed to warm to room temperature and stirred for 4 h at the same temperature. Then the indenyi lithium suspension was cooled again to -50°C and added of a solution of 1,2-dibromoethane (0.24 mol, 21 mL) in 50 mL of ether. The reaction mixture was allowed to warm up slowly to room temperature and stirred overnight Then it was treated with a saturated aqueous solution of NH4CL The organic phase was isolated, evaporated off to dryness and distilled in vacuo, b.p. 110°C/0,5 torr. Yield 21.6 g (60%). The title compound was characterized by NMR spectroscopy. Synthesis of l^-(3-indenyI)-7-(2^-dimethylcyclopenta[l^-b:4^-b']-dithiophene)ethane A solution of 2,5-dimethylcyclopenta[l,2-b:4,3-b']-dithiophene (1.03 g, 5 mmol) in 50 mL of THF was treated at -70°C with a 1.6 M w-BuLi solution in hexane (3.1 mL, 5 mmol). The resulting mixture was stirred for additional 45 min at 0°C, then cooled again to ~-70°C and treated with l-bromo-2-(3-indenyl)ethane (1.12 g, 5 mmol) in 25 mL of THF. The reaction mixture was allowed to warm to room temperature and subsequently treated with a saturated aqueous solution of NH4CI. The organic phase was isolated and the solvents were removed. The residue was passed through a column packed with silica gel by using hexane as eluent Yield L26 g (72%). The title compound was characterized by NMR spectroscopy. Synthesis of ethylidene^l-indenyl^^S-dimethylcyclopentatl^-b^^-b5]- dithiophene)hzirconium dichloride C-37 A solution of l,2-(3-indenyl)-7-(2,5-dimethylcyclopen^ (1.26 g, 3.62 mmol) in 15 mL of ether and 60 mL of hexane was treated at -70°C with a 1.6 M n-BuIi solution in hexane (AH mL, 7.5 mmol). The resulting suspension was stiiTed for additional 2 h at room temperature, then cooled again to -70°C and added of ZrCU (0.94 g, 4 mmol). The reaction mixture was allowed to warm to room temperature and stirred overnight The dark orange precipitate was filtered, washed twice with ether, dried and then recrystallyzed from CH2C12. Yield 0.92 g (50%). ^-NMR (5, ppm, CD2CI2): 7.70 (dd, 1H, CH); 7.45 (dd, 1H, CH); 7.20 (m, 1H, CH); 7.10 (m, 1H, CH); 6.75 (q, 1H, CH); 6.60 (q, 1H, CH); 6.55 (dd, 1H, CH); 6.40 (d, 1H, CH); 3.95- 3.80 (m, 2H, CH2); 3.65-3.55 (m, 2H, CH2); 2.60 (d, 3H, CH3); 2.45 (d, 3H, CH3). EXAMPLE 31 Synthesis of cUoro(497-dimethyI-l-indenyl)dimethylsilane The precursor 4,7-dimethylindene was prepared by following standard procedure (as reported in Tetrahedron, 51, (1995), 4347). A 1.6 M 7Z-BuLi solution in hexane (62.5 mL, 0.1 mol) was added at 0°C to a solution of 4,7- dimethylindene (14.42 g, MW = 144.22, 0.1 mol) in 200 mL of hexane and 50 mL of THF. The resulting suspension was allowed to warm to room temperature and stirred for 4 h at the same temperature. Then the indenyl lithium suspension was cooled again to -50°C and added of a solution of dichlorodimethylsilane (0.2 mol, 24 mL) in 50 mL of THF. The resulting suspension was allowed to warm to room temperature and stirred overnight The precipitate of lithium chloride was filtered, the filtrate was evaporated off to dryness and distilled in vacuo, b.p. 98°C/0.5 torr. Yield 16.5 g (70%). The title compound was characterized by NMR spectroscopy. Synthesis of (4,7-dimethyl-l-md^ dithiophene)dimethylsilane A solution of 2^-diiiie&ylcyclopenta[l,2-b:43-b']-dithiophene (1.90 g, 92 mmol) in 50 mL of ether was treated at -70°C with a 1.6 M ra-BuLi solution in hexane (5.8 mL, 9.2 mmol). The resulting mixture was stirred for additional 45 min at 0°C, then cooled again to -70°C and treated with chloro(4,7-dimethyH-indenyI)dimethylsilane (2.18 g, 9.2 mmol) in 10 mL of ether. The reaction mixture was allowed to warm to room temperature and subsequently treated with a saturated aqueous solution of NH4CI. The organic phase was isolated and the solvents were removed. The residue was recrystallysed from hexane. Yield 3.67 g (98%). 'H-NMR (8, ppm, CDCI3): 7.07 (dd, 1H, CH); 7.05 (d, 1H,.CH); 6.95 (d, 1H, CH); 6.90 (m, 2H, CH); 6.60 (dd, 1H, CH); 4.00 (s, 1H, CH); 3.85 (s, 1H, CH); 2.64 (s, 3H, CH3); 2.60 (s, 3H, CH3); 2.50 (s, 3H, CH3); 2.40 (s, 3H, CH3); -0.20 (s, 3H, Si-CH3); -0.40(s, 3H, Si-CH3). Synthesis of dimethybilyri (4,7-dmetty^ b']-dithiophene)hrirconium dichloride C-38 A solution of (4,7-dmethyM-mdeny^ dithiophene)dimethyisilane (3.67 g, 9.02 mmol) in 15 mL of ether and 50 mL of hexane was treated at -70°C with a 1.6 M w-BuLi solution in hexane (12.5 mL, 20 mmol). The resulting suspension was stirred for additional 2 h at room temperature, then cooled again to -70°C and added of ZrCU (2.52 g, 10.8 mmol). The reaction mixture was allowed to warm to room temperature and stirred overnight. The yellow precipitate was filtered, washed twice with ether, dried and then reciystallyzed from CH2CI2. Yield 3.57 g (70%). The title compound was characterized by NMR spectroscopy. EXAMPLE 32 Synthesis of t:hloro(2,497-trimethyH-mdenyl)dimethylsilane The precursor 2,4,7-trimethylindene was prepared by following standard procedure (as reported in Eur. Pat AppL 0693506). A 1.6 M n-BuLi solution in hexane (37.5 mL, 60 mmol) was added at 0°C to a solution of 2,4,7-trimethylindene (9.5 g, MW = 158.24, 60 mmol) in 200 mL of hexane and 50 mL of THF. The resulting suspension was allowed to warm to room temperature and stirred for 4 h at the same temperature. Then the indenyl lithium suspension was cooled again to -50°C and added of a solution of dichlorodimethylsilane (90 mmol, 11 mL) in 50 mL of THF. The resulting suspension was allowed to warm to room temperature and stirred overnight The precipitate of lithium chloride was filtered, the filtrate was evaporated off to dryness and distilled in vacuo, b.p. 110°C/0.5 torr. Yield 10.1 g (67%). ^-NMR (5, ppm, CsDe): 6.75 (d, 1H, CH); 6.60 (d, 1H, CH); 6.30 (s, 1H, CH); 3.25 (s, 1H, CH); 2.25 (s, 3H, CH3); 2.15 (s, 3H, CH3); 2.10 (s, 3H, CH3); -0.05 (s, 3H, Si-CH3); -0.02 (s, 3H, Si-CH3). Synthesis of (2,4J-trimethyl-l-tad^ dithiophene)dimethylsilane A solution of 2,5-dimethylcyclopenta[l:t2-b:4,3-b']-dithiophene (1.65 g, 8 mmol) in 50 mL of ether was treated at -70°C with a 1.6 M n-Buli solution in hexane (5.0 mL, 8 mmol). The resulting mixture was stirred for additional 45 mm at 0oC, then cooled again to -70°C and treated with cUoro(2»4,7-trimethyl-l-indenyl)dimethylsilan^ (2.0 g, 8 mmol) in 20 mL of ether. The reaction mixture was allowed to warm to room temperature and subsequently treated with a saturated aqueous solution of NEUC1. The organic phase was isolated and the solvents were removed. Yield 3.36 g (-100%). XH-NMR (5, ppm, CDCI3): 6.90 (d, 1H, CH); 6.80 (d, 1H, CH); 6.70 (m, 2H, CH); 6.65 (m, 1H, CH); 4.15 (s, 1H, CH); 4.00 (s, 1H, CH); 2.65 (s, 3H, CH3); 2.63 (s, 3H, CH3); 2.55 (s, 3H, CH3); 2.50 (s, 3H, CH3); 2.20 (s, 3H9 CH3); -0.15 (s, 3H, Si-CH3); -0.30 (s, 3H, Si-CH3). Synthesis of dimethylsilytf (2,4,7-t^ b']-dithiophene) ^zirconium dichloride C-39 A solution of (2,4,7-trimethyl-l"indenyl)-7-^ dithiophene)dimethyisilane (3.36 g, 8.0 mmol) in 80 mL of ether was treated at ~70°C with a 1.6 M n-BuIi solution in hexane (12.5 mL, 20 mmol)* The resulting suspension was stirred for additional 2 h at room temperature, then cooled again to -70°C and added of ZrCL* (2.34 g, 10 mmol). The reaction mixture was allowed to warm to room temperature and stirred overnight The orange precipitate was filtered, washed twice with ether, dried and then recrystallyzed from CH2CI2. Yield 2.73 g (59%). The title compound was characterized by NMR spectroscopy. EXAMPLE 33 Synthesis of 2-methyl-293-dihydro-lH-cyclopenta[a]naphtalen-l-one To a suspension of A1C13 (85 g, 0.635 mol) in 200 mL of CH2C12 were added at 0°C first naphalene (32.5 g, 0.254 mol) and then a solution of 2-methylacryloyl chloride (26.5 g, 0.254 mol) in 50 mL of CH2CI2. The reaction mixture was stirred for 30 min at 0°C, then 2 h at room temperature and finally poured into a mixture of ice and water. The dark organic layer was separated, while the water layer was extracted with CHCI3 (3 x 150 mL). The organic layers were collected, washed with potassium caibonate/water until neutral pH, dried over MgS04 and evaporated off to dryness. Yield 28.09 g (56%). The title compound was characterized by NMR spectroscopy. Synthesis of 2-methyl-2?3- A solution of 2-methyl-2,3-dihydro-lH-cyclopenta[a]nq)htalen-l-one (28.09 g, 0.143 mol) in 100 mL of THF was slowly added to a suspension of L1AIH4 (2.18 g, 58 mmol) in 200 mL of ether and refluxed for 2 h under stirring. The reaction mixture was subsequently transferred into a 2-L beaker and slowly hydrolyzed, under constant stirring, by dropwise addition of a 10% aq. solution of HC1 until pH 5. The organic layer was separated, while the water layer was extracted with ether (3 x 100 mL). The organic layers were collected, washed with potassium carbonate/water until neutral pH, dried over MgS04 and evaporated off to dryness. The so-obtained product, as a mixture of two isomers, was used in the next step without further purification. Synthesis of 2-methyI-3H-cyclopenta[a]uaphtalene A mixture of 2-methyl-2,3Hlihydro-lH-cyclopen1a[a]iiaphthalen-l-ol (obtained as described above) and 1 g ofp-toluenesulphonic acid in 200 mL of benzene was refluxed for 1 h. Then the reaction mixture was cooled to room temperature and treated with a saturated aqueous solution of Na2C03. The organic phase was isolated, dried over MgSC>4 and evaporated off to dryness. Yield 14.2 g (55% based on starting 2-methyl-2,3-dihydro-lH-cyclopenta[a]naphtalen-l-one). !H-NMR (5, ppm, CDC13): 8.10-7.40 (m, 6H, CH); 7.10 (s, 1H, CH); 3.50 (s, 2H, CH2); 2.33 (s, 3H, CH3). Synthesis of chloro(2-methyl-3H-cyclopenta[a]naphthalen-3-yl)dimethylsilane A 1.6 M n-BuLi solution in hexane (7.5 mL, 12 mmol) was added at -50°C to a solution of 2-methyl-3H-cyclopenta[a]naphthalene (2.14 g, MW = 180.25, 11.9 mmol) in 50 mL of ether. The resulting suspension was allowed to warm to room temperature and stirred for 45 -min at the same temperature. Then the lithium suspension was cooled again to -70°C and added of dichlorodimethylsilane (18 mmol, 2.2 mL). The reaction mixture was allowed to warm to room temperature and stirred overnight The precipitate of lithium chloride was filtered, the filtrate was evaporated off to dryness and dried in vacuo. Yield 3.14 g (97%). lH-NMR (5, ppm, CeDe): 8.10 (d, 1H, CH); 7.85 (d, 1H, CH); 7.50-7.40 (m, 4H, CH); 7.10 (s, 1H, CH); 3.55 (s, 1H, CH); 2.30 (s, 3H, CH3); 0.22 (s, 3H, Si-CH3); -0.05 (s, 3H, Si-CH3). Synthesis of (2-methylcyclopenta[a]naphthalen-3-yl)-7-(2,5-dimethylcyc]openta[l,2-b:4,3-b']-dithiophene)dimethylsilane A solution of 2,5-dimethylcyclopenta[l^-b:4,3-b']-dithiophene (2.37 g, 11.5 mmol) in 75 mL of ether was treated at -70°C with a 1.6 M rt-BuIi solution in hexane (7.5 mL, 12 mmol). The resulting mixture was stirred for additional 45 min at 0°C, then cooled again to -70°C and treated with cMoro(2-methyl-3H-cyclopenta[a]naphthalen-3-yl)dimethylsilane (3.14 g, 11.5 mmol) in 25 mL of ether. The reaction mixture was allowed to warm to room temperature and subsequently treated with a saturated aqueous solution of NH4CI. The organic phase was isolated and the solvents were removed. The residue was passed through a short column packed with silica gel by using hexane as eluent. Yield 4.07 g (80%). JH-NMR (8, ppm, CDC13): 8.20 (d, 1H, CH); 8.00 (d, 1H, CH); 7.70-7.40 (m, 4H, CH); 6.95 (d, 2H, CH); 6.80 (s, 1H, CH); 4.20 (s, 1H, CH); 4.15 (s, 1H, CH); 2.66 (s, 6H, CH3); 2.45 (s, 3H, CH3); -0.27 (s, 3H, Si-CH3); -0.29 (s, 3H, Si-CH3). Synthesis of dimethylsayl^Z-methylcyclopentalaJnaphthalene^T-CZ^ dimethylcyclopenta[l^-b;43-b']-dithiophene)l>zirconium dichloride C-40 A solution of (2-metliylcyclopmta[a]naphtM b']-ditfaiophene)dimethylsilane (4.07 g, 9.2 mmol) in 100 mL of ether was treated at -70°C with a 1.6 M n-BuLi solution in hexane (15 mL, 24 mmol). The resulting suspension was stirred for additional 2 h at room temperature, then cooled again to -70°C and added of ZrCU (2.79 g, 12 mmol). The reaction mixture was allowed to warm to room temperature and stirred overnight. The orange precipitate was filtered, washed twice with ether, dried and then recrystallyzed from CH2C12. Yield 2.77 g (50%). lH-NMR (S, ppm, CD2CI2): 8.00 (d, 1H, CH); 7.70 (d, 1H, CH); 7.60 (d, 1H, CH); 7.55 (t, 1H, CH); 7.48 (t, 1H, CH); 7.25 (s, 1H, CH); 7.15 (d, 1H, CH); 6.78 (q, 1H, CH); 6.65 (q, 1H, CH); 2.60 (d, 3H, CH3); 2.55 (d, 3H, CH3); 2.40 (d, 3H, CH3); 1.32 (s, 3H, Si-CH3); 1.18 (s, 3H, Si-CH3). EXAMPLE 34 Synthesis of dimethylsilyH (l-indenyI)-7-(2,5-ditrimethylsflyl-cyclopenta[l?2-b:43-b'l- dithiophene)} zirconium dichloride C-13 The C13-ligand synthesis was carried out by coupling the lithium salt of 2,5-ditrimetihylsilyl-7H-cyclopenta[l^-b:4,3-b']dilhiophene with chloro(l-indenyl)dimethyl silane. A suspension of 1.48 g (3 mmol) of (l-indenyl)-7^(2,5^1rimethylsilyl-cyclopenta[lr2-b:4,3-b']dithiophene) Mimetbylsilane in 50 mL of ether was treated at -70°C with 4.1 mL of a 1.6 M n-BuIi solution (6.5 mmol). After the addition, the reaction mixture was allowed to warm to 0°C and added of 0.75 g (3.2 mmol) of ZrCL*. The resulting mixture was allowed to reach room temperature and stirred overnight Then the red precipitate obtained was filtered, washed twice with ether, dried and finally recrystallyzed from CH2C12. Yield 1.38 g (70%). JH-NMR (5, ppm, CD2CI2): 7.90-6.90 (m, 7H, CH); 6.10 (m, 1H, CH); 1.40 (s, 3H, Si-CH3); 1.10 (s, 3H, S1-CH3); 0.41 (s, 9H, Si(CH3)3); 0.20 (s, 9H, Si(CH3)3). EXAMPLE 35 Synthesis of (3-methyl-4-trimethylsilyl-l-cyclopentadienyl)-7-(2?5-dimethyl- cyclopenta[l?2-b:4r3-b,]-dithiophene)dimethylsilaBe A solution of 1.03 g (5.0 mmol) of Z^-dimethyl-TH-cyclopentatl^-b^^-b'J-dithiophene in 40 mL of ether was treated at -70°C with 3.13 mL of a 1.6 M n-BuLi solution (5.0 mmol). After the addition, the mixture was allowed to warm to room temperature and stirred for additional 1 h at this temperature. Then it was cooled again to -70°C and added of a solution of 1.22 g (5 mmol) of chlorodimethyl(3-methyl^trim^^ in 10 mL of ether. The resulting mixture was allowed to reach room temperature and stirred overnight The ligand (3-methyl^trimethylsi^ c^clopenta[l^-b:4,3-b,]-dithiophene)dimethylsilane was not isolated, but used in solution for the catalysts synthesis (see below). Synthesis of dimethylsflyl{(3-methyl^trimeto^ dimethyl-cyclopenta [lr2-b:43-b']-dithiophene)} zirconium dichloride [C-32] The ligand solution coming from the previous step was treated at -70°C with 6.3 mL of a 1.6 M w-BuIi solution (10.1 mmol). After the addition, the reaction mixture was allowed to reach room temperature and stirred for additional 50 min at this temperature. The solvent was removed under reduced pressure and the dilithium salt obtained was suspended in hexane. After cooling to -70°C, 1.17 g (5.0 mmol) of ZrCU were added. The reaction mixture was stirred at room temperature overnight, the yellow precipitate was filtered, washed twice with hexane, dried and finally recrystallized from Et20. Yield 0.90 g (31%). JH-NMR (8, ppm, CD2C12): 6.95 (q, 1H, CH, J = L17 Hz); 6.91 (q, 1H, CH, J = 1.17 Hz); 5.77 (d, 1H, CH, J = 2.74 Hz); 5.68 (d, 1H, CH, J = 2.74 Hz); 2.62 (q, 3H, CH3, J = 1.17 Hz); 2.59 (q, 3H, CH3, J = 1.17 Hz); 2.22 (s, 3H, CH3); 0.91 (s, 3H, Si-CH3); 0.89 (s, 3H, Si-CH3); 0.22 (s, 9H, SKCH3)3). POLYMERIZATION EXAMPLES General procedures The cocatalyst methylalumoxane (MAO) was a commercial product which was used as received (Witco AG, 10 %wt/vol toluene solution, 1.7 M in Al). The catalyst mixture was prepared by dissolving the desired amount of the metallocene with the proper amount of the MAO solution, obtaining a solution which was stirred for 10 min at ambient temperature before being injected into the autoclave. Polymerization examples 1-33 propylene polymerization 1 mmol of Al(z-Bu)3 (as a 1M solution in hexane) and 290 g of propylene were charged at room temperature in a 1-L jacketed stainless-steel autoclave, equipped with magnetically driven stirrer and a 35-mL stainless-steel vial, connected to a thermostat for temperature control, previously purified by washing with an Al(i-Bu)3 solution in hexanes and dried at 50°C in a stream of propene. The autoclave was then thermostatted at 2 °C below the polymerization temperature, and then the toluene solution containing the catalyst/cocatalyst mixture was injected in the autoclave by means of nitrogen pressure through the stainless-steel vial, the temperature rapidly raised to the polymerization temperature and the polymerization carried out at constant temperature for 1 hour. After venting the unreacted monomer and cooling the reactor to room temperature, the polymer was dried under reduced pressure at 60 °C. The polymerization conditions and the characterization data of the obtained polymers are reported in Table 1. Polymerization example 34 propylene/butene copolvmerization Operating as in the case of propylene homopolymerizations, 1 mmol of Al(z-Bu)3 (as a 1M solution in hexane), 160 g of propylene and 154 g of 1-butene were charged at room temperature in the 1-L jacketed stainless-steel autoclave, thermostatted at 58 °C, in order to have a 50/50 mol% in the liquid phase, and then the toluene solution containing the catalyst/cocatalyst mixture (0.5 mg of C-20, 0.45 mmol of MAO, in 3 mL of toluene) was injected in the autoclave by means of nitrogen pressure through the stainless-steel vial, the temperature rapidly raised to the polymerization temperature and the polymerization carried out at constant temperature for 1 hour. 26.5 g of essentially amorphous polymer were recovered, which has LV. = 2.29 dL/g, Tg = -13.6 °C, and butene = 27.7 wt% (22.3 mol%). Polymerization example 35 propylene/ethylene copolvmerization Operating as in the case of propylene homopolymerizations, 1 mmol of Al(/-Bu)3 (as a 1M solution in hexane), propylene and ethylene were charged at room temperature in the 1-L jacketed stainless-steel autoclave, thermostatted at 58 °C, in order to have a liquid phase composition of 288 g propylene and 1.5 g ethylene (0.42 %wt) in the liquid phase, and then the toluene solution containing the catalyst/cocatalyst mixture (0.3 mg of C-20, 0.27 mmol of MAO, in 3 mL of toluene) was injected in the autoclave by means of nitrogen pressure through the stainless-steel vial, the temperature rapidly raised to the polymerization temperature and the polymerization carried out at constant temperature and pressure (25 bar-g) by feeding ethylene (13.3 g total absorption) for 1 hour. 52.7 g of essentially amorphous polymer were recovered, which has IV. = 1.23 dL/g, and ethylene = 6.3 wt% (9.2 mol%). Polymerization example 36 propylene polymerization with supported catalyst a) Preparation of the supported catalyst The apparatus used for the supportation is a glass cylindrical vessel mechanically stirred in order to allow a good mixing between the carrier and the catalytic solution during the impregnation operation. 6 g of a porous polyethylene having LV. 21 dL/g, mean Particle size 386 \mx and porosity 50,9 % VN (L07 cc/g) was loaded into the vessel and mechanically suspended under nitrogen flow. The catalytic solution was prepared by dissolving 24 mg of C-20 in 12 mL of a MAO solution (WTTCO , lOOg/L in toluene). Due to the limited porosity of the carrier die liquid is dropped onto the solid until the incipient wetness condition is reached. At this point the solvent is evaporated off under vacuum. All the operations are carried out at room temperature. The catalytic solution is then added to the carrier step by step. The final catalyst appears as a pink-violet free flowing solid with the following composition: Al 5.0%w and Zr 0.0705%w (Al/Zr molar ratio 240). b) Polymerization A 4L stainless-steel reactor, equipped with a blade turbine magnetic stirrer, pressure indicator, temperature indicator and a thermosetting jacket, was used. A batch polymerization was carried with the following procedure. 1200 g of liquid monomer was loaded at 30 °C, followed by 3 ml of a TDBA solution 100 g/1 in hexane used as a scavenger. The polymerization was started by injecting 305 mg of the catalyst into the autoclave at 30°C, by means of nitrogen overpressure, then the temperature was raised up to 60°C in 10 minutes and maintained for 1 hour. The polymerization was stopped by venting and cooling the reactor. No significant fouling was observed. The product obtained was collected and dried in an oven flushed with nitrogen at 70°C for 3 hours. 360 g of polymer- was obtained with a good morphology having an LV. of 1.94 dL/g. The activity of the catalyst was 1.2 kgPP/g cat supp.h, corresponding to 1.7ton PP/gZrix. d) Physical characterization The polymer was additivated with the reported stabilisation formula and pelletised with the following processing parameters: Cylinder Temperature: 230 °C Feeding Temperature: 230 °C Screw speed: 50 rpm The so obtained pellets were compression moulded with Carver press Compression moulding: Plaque thickness: Haze, Gloss, DMTA: LOmm Tensile test: 2,0 mm Notched Izod: 3.2 mm Press Plaque Temperature: 200 °C Preheating time (no press): 5 min Pressure time: 5 min Pressure: 14 bar Cooling: rapid in ice/water bath The plaques, after compression moulding were stored at room temperature at least 48 hours before characterisation. DSC measurement, obtained with a Metfler calorimeter with the following procedure: First run: Heating the sample from -120 to 200°C at 20°C/min Crystallisation: Cooling from 200°C to -120°C at 20°C/min Second nm: Heating the sample from -120 to 200°C at 20°C/min The physical characterization of the polymer is reported at table 2. Polymerization examples 37-59 ethylene/propylene polymerization The Ethylen Propylene mixtures were prepared in a 5 L steel cylinder, filled with quantities of the two gases small enough to prevent their condensation. The composition of the gaseous mixture in the cylinder was controlled through GC analysis. The copolymerizations were carried out at 50 °C in a 250 mL glass reactor equipped with a mechanical stirrer, an AlHhn condenser, a thermometer and a pipe for monomers feeding, and kept in a thermostatic bath. First, 100 mL of toluene and 3.5 mmol of TTOAO solution were introduced into the nitrogen-purged reactor. At the polymerization temperature, the nitrogen was removed and replaced with the comonomers mixture, with a flow rate of 1.5 L/min. When the equilibrium pressure (1.1 atm of total pressure) was reached, 3.5 )imol of the metallocene dissolved in 5 mL of hexane in the presence of a 35 |xmol of TIOA (35 jiL of solution 1 M), was added to start the polymerization. During the reaction, the temperature was kept within 50 ± 1 °C. After 15 min the polymerization was quenched by adding 1 mL of methanol, and the copolymer was precipitated with 300 mL of methanol acidified with HC1, filtered, washed and dried overnight in vacuo at 50 °C. Polymerization results characterization and reactivity ratios rl and r2 of ethylene/propylene copolymers are reported in tables 3,4 and 5. Polymerization example 60 ethylene polymerization with supported catalyst A 4L stainless-steel reactor, equipped with a blade turbine magnetic stirrer, pressure indicator, temperature indicator, feed line for monomer equipped with a thermal-mass flowmeter for the measure of the ethylene uptake and a thermosetting jacket, was used. A batch polymerization was carried out with the following procedure. 1600 ml of liquid propane is loaded into the reactor at 30°C, followed by 2.5 mmoles of tri-isobutylaluminum as the scavenger. The autoclave was pressurized with an ethylene partial pressure of 5 bar. The polymerization was started by injecting 162 mg of the catalyst prepared in example 37 a) into the autoclave at 30°C, by means of nitrogen overpressure. A prepolymerization step was carried out at 30°C for 30 minutes. After this time the reactor temperature was incresaed up to 75°C and the ethylene partial pressure also was increased to 10 bar. The polymerization was stopped after 2 hours by venting and cooling the reactor. The polymer discharged was dried in an oven flushed with nitrogen at 70°C for 3 hours. 90 g of polymer was obtained with an intrinsic viscosity of 4.29 dL/g and a melting temperature of 141.4° C. WE CLAIM: 1. A metallocene compound of general formula (T): LGZMXp (I) wherein L is a divalent group bridging the moieties G and Z, selected from CR1R2, SiR1R2 and (CRlR2)2, R1 and R2, which may be the same as or different from each other, are selected from hydrogen, a C1-C20-alkyl, C3-C20-cycloaIkyl, C2-C20-alkenyl, C6-C20-arryl, C7-C20-aIkylaryl, C7-C20rarylalkyI radical, optionally containing a heteroatom, which can form a ring having 3 to 8 atoms which can bear a substituent; Z is a moiety of formula (II): wherein R3 and R4, which may be the same as or different from each other, are selected from a C1-C20-alkyl, C3-C20-cycloalkyl, C2-C20-alkenyl, C6-C20-aryl, C7-C20-alkylaryl, C7-C20-arylalkyl radical, optionally containing a heteroatom; A and B are selected from sulfur (S), oxygen (O) or CR5, wherein R5 is selected from hydrogen, a C1-C20-alkyl, C3-C20-cycloalkyl, C2-C20-alkenyI, C6-C20-aryl, C7-C20-alkylaryl, C7-C20-arylalkyl radical, optionally containing a heteroatom with the proviso that if A is S or O, then B is CR5 or if B is S or O, then A is CR5, and wherein the rings containing A and B have a double bond in the allowed position; G is a moiety of formula (HI): wherein R6, R7, R8 and R9, which may be the same as or different from each other, are selected from hydrogen, a C1-C20-alkyl, C3-C20-cycloa]kyl, C2-C20-alkenyl C6-C20aryl, C7-C20-alkylaryl, C7-C20-arylalkyl radical, optionally containing containing heteroatoms belonging to groups 13-17 of the Periodic Table of the Elements, and R6 and R7 and/or R8 and R9 can form a ring comprising from 3 to 8 atoms, which can bear substituents, with the proviso that R is different from R8 and when R9 is a tert-butyl radical, R8 is not hydrogen; M is an atom of a transition metal selected from those belonging to group 3,4,5,6 or to the lanthanide or actinide groups in the Periodic Table of the Elements (new IUPAC version), X, which may be the same or different, is selected from hydrogen atom, halogen atom, a group R10, OR10, OSO2CF3, OCOR10, SR10, NR102 or PR102, wherein the substituents R10 are selected from hydrogen, a C1-C20-alkyl,- C3-C20-cycloalkyl, C2-C20-aIkenyl C6-C20-aryl, C7-C20-alkylaryl, C7-C20-arylalkyl radical, optionally containing heteroatoms; p is an integer of from 1 to 3, being equal to the oxidation state of the metal M minus 2; isopropylidene (3-trime1hylsnylcyclopentadienyl)(7-cyclopentaditiophene)zirconium dichloride, dimethylsilanediyl (3-trimethylsilylcyclopentadienyl)(7- cyclopentaditiophene)zirconium dichloride, isopropylidene (3-ethyicyclopentadienyl)(7- cyclopentaditiophene)zirconium dichloride, dimethylsilanediyl (3- ethylcyclopentadienyiX7^yclopentaditiophene)zirconium dichloride, isopropylidene (3- n-butylcyclopentadienyl)(7-cyclopentaditiophene)zirconium dichloride, dimethylsilanediyl (3-n-butylcyclopentadienyl)7-cyclopentaditiophene)zirconium dichloride, isopropylidene (3-methylcyclopentadienyl)(7- cyclopentaditiophene)zirconium dichloride, dimethylsilanediyl (3- methylcyclopentadienyl)(7-cyclopentaditiophene)zirconium dichloride, isopropylidene (3-i-propyIcyclopentadienyO(7-cyclopentaditiophene)zirconium dichloride and dimethylsilanediyl (34-propylcyclopentadienylX7-cyclopentaditiophene)zirconium dichloride being excluded. 2. The metallocene according to claim 1, wherein the transition metal M is selected from titanium, zirconium and hafiuum. 3. The metallocene according to any of claims 1 to 2, wherein L is CMe2 or SiMe2. 4. The metallocene according to any of claims 1 to 3, wherein A or B is a sulfur atom and the other is a CH group. 5. The metallocene according to any of claims 1 to 4, wherein R3 and R4 are the same and are selected from a C1-C20-alkyl group, which can contain a silicon atom. 6. The metallocene according to any of claims 1 to 5, wherein G is a moiety of formula (IIIa): wherein R6 and R9 equal to or different from each other, are selected from hydrogen, a C1-C20-alkyl, C3-C20-cycloalkyl, C2-C20-alkenyl, C6-C20-aryl, C7-C20-alkylaryl, C7-C20-arylalkyl radical, optionally containing heteroatoms belonging to groups 13-17 of the Periodic Table of the Elements R7 is selected from a C6-C20-aryl C7-C20-alkylaryl or a QR11R12R13 group, wherein Q is selected from C, Si, Ge; R11, R12 and R13, which may be the same as or different from each other, are hydrogen, C1-C20-alkyl, C3-C20cycloalkyl, C2-C20-aIkenyl, C6-C20-aryl, C7-C20-aIkylaryl, C7-C20-arylalkyl radicals, optionally containing a heteroatom, with the proviso that when Q is a carbon atom, at least one of R11, R12 and R13 is a hydrogen atom. 7. The metallocene according to claim 6, wherein R7 is selected from phenyl, a CHR11R12 and a SiR11R12R13 group, wherein R11, R12 and R13 are hydrogen or C1-C20-aIkyl groups. 8. The metallocene according to any of claims 1 to 5, wherein G is a moiety of formula (IV): wherein T1 is a sulfur atom or a CR16 group; T is a carbon atom or a nitrogen atom; z is 1 or 0; the ring containing Tl and T2 has double bonds in the allowed position; with the proviso that if z is 1, T1 is a CR16 group and T2 is a carbon atom and the ring formed is a benzene ring and if z is 0, T2 bonds directly the cyclopentadienyl ring, the 5 membered ring formed has double bond in any of the allowed position having an aromatic character and T1 and T2 are not at the same time, a sulfur atom and a nitrogen atom. R14, R15, R16, R17, R18 and R19, same or different, are selected from hydrogen, a C1-C20-alkyl, C3-C20-cycloalkyl, C2-C20-alkenyl, C6-C20-aryl, C7-C20-alkylaryl, C7-C20crarylalkyl radical, optionally containing heteroatoms belonging to groups 13-17 of the Periodic Table of the Elements, any of two adjacent R14, R15, R16, R17, R18 and R19 can form a ring comprising 4 to 8 atoms which can bear substituents. 9. The metallocene according to claim 8, wherein G is a moiety of formula (IVb): wherein R14, R15, R16, R17, R18 and R19, which may be Hie same as or different from each other, are selected from hydrogen, a C1-C20-alkyl, C3-C20-cycloalkyl, C2-C20-alkenyl, C6-C20-aryl, C7-C20-alkylaryl, C7-C20-arylalkyl radical, optionally containing heteroatoms, and any of two adjacent R14, R15,- R16, R17, R18 and R19 can form a ring comprising 4 to 8 atoms which can bear substituents and the benzene ring can be perhydrated. 10. The metallocene according to claim 9, wherein G is a moiety of formula (IVb) wherein R15, R16, R17, and R18 are selected from hydrogen, a C1-C20-alkyl, C3-C20-cycloalkyl, C2-C20-aIkenyl, C6-C20-aryl, C7-C20-alkylaryl C7-C20-arylaIkyl radical, optionally containing heteroatoms belonging to groups 13-17 of title Periodic Table of the Elements, and any of two adjacent R14, R15, R16, R17, R18 can form a ring comprising 4 to 8 atoms which can bear substituents; R14 is selected fiom the group consisting of C1-C20-aIkyl or C6-C20-aryl group. 11. The metallocene according to claim 9, wherein G is a moiety of formula (IVc) wherein R14, R16, R17, and R18 are selected fiom hydrogen, a C1-C20alkyl, C3-C20-cycloalkyl, C2-C20-aIkenyl, C6-C20-aryl C7-C20-alkylaryl, C7-C20-alylalkyl radical, optionally containing heteroatoms belonging to groups 13-17 of the Periodic Table of the Elements, and optionally any of two adjacent R14, R16, R17, R18 and R19 can form a ring comprising 4 to 8 atoms which can bear substituents;; R19 is selected fiom the group consisting of C1-C20-aIkyl or C6-C20-aryl group or forms with R18 a benzene ring that can bears substituents. 12. The metallocene according to claim 11, wherein R14 is selected fiom the group consisting of C1-C20-aIkyl or C6-C20-aryl group such as a methyl, ethyl, or phenyl group. 13. The metallocene according to any of claima 11-12, wherein R16 is selected fiom the group consisting of C1-C20-aIkyl or C6-C20-aryl. 14. The metallocene according to claim 8, wherein G is a moiety of formula (TVd): wherein T1 is a sulfur atom or a CR16 group; T2 is a carbon atom or a nitrogen atom; the 5 member ring formed by T1 and T2 has double bonds in any of the allowed position, having an aromatic character; with the proviso that if T1 is a sulphur atom T2 is not a nitrogen atom; R14, R17 and R18 which may be the same as or different from each other, are selected from hydrogen, a C1-C20alkyl C3-C20-cycloaIkyl, C2-C20alkenyl, C6-C20-aryl, C7-C2o-alkylaiyl, C7-C2o-a*ylalkyl radical, optionally containing heteroatoms belonging to groups 13-17 of the Periodic Table of the Elements and Rl7and R18 can form a ring comprising 4 to 8 atoms which can bear substituents. 15. The metallocene according to claim 14 wherein T2 is a carbon atom; Tl is a sulphur atom and R14, R17 and R18 equal to or different from each other are C1-C20-alkyl, C6-C20aryl. 16. A ligand of formula (V): LG'Z' (V) wherein L is defined as in claims 1-5: Z' is a moiety of formula (VI): and its double bound isomers; wherein A, B, R3 and R4 are defined as in claims 1-5 and the double bonds are in any of the allowed positions; G' is a moiety of formula (VH): and its double bond isomers; wherein R6,R7,R8 and R9 have the meaning as defined in any of claims 1 to 5. 17. A process for the preparation of a ligand of formula (V): LG'Z' (V) wherein G\ Z' and L are defined as in claim 16; comprising the following steps: a) contacting a compound of the formula (VIH) with abase selected from the group consisting of metallic sodium and potassium, sodium and potassium hydroxide and an organic lithium compound, wherein the molar ratio between the compound of the formula (VIE) and said base is at least 1:1; wherein A, B, R3 and R4 are described in claims 1-5; b) contacting the corresponding anionic moiety of the formula (VD3) with a compound of formula (K): wherein R1, R2, R6, R7, R8 and R8 are described in claim 1 and then treating the obtained product with a protonating agent 18. A process for the preparation of a ligand of formula (V): LG'Z' (V) wherein L, G' and Z' are defined as in claim 16 are defined in claim 1 comprising the following steps: a) contacting a compound of the formula (VIE) with a base selected from the. group consisting of metallic sodium and potassium, sodium and potassium hydroxide and an organic lithium compound, wherein the molar ratio between the compound of the formula (VET) and said base is at least 1:1 (VIE) wherein A, B, R3 and R4 are described as in claims 1-5; b) contacting the obtained anionic compounds of the formula (VIII) with a compound of formula (IX): wherein L, R6, R7, R8 and R9 are defined as in claims 1-5 and Y is a halogen radical selected from the group consisting of chloride, bromide and iodide. 19. A process for the preparation of a metallocene compound as defined in any of claims 1 to 15, obtainable by contacting- the ligand of general formula (V) with a base capable of forming the corresponding dianionic compound and thereafter with a compound of general formula MXp+2, wherein M, X and p are defined as in claims 1-5. 20. A catalyst obtainable by contacting: (A) a metallocene compound of formula (T) LGZMXp (T) wherein L, Z, M, X, and p has been defined as in claims 1-5 and G is a moiety of formula (ID): wherein R6, R7, R8 and R9, which may be the same as or different from each other, are selected from the group consisting of hydrogen, a C1-C20-alkyl, C3-C20cycloalkyl, C2-C20-alkenyl, C6-C20-aryl, C7-C20aIkylaryl, C7-C20arylalkyl radical, optionally containing heteroatoms belonging to groups 13-17 of the Periodic Table of the Elements, R6 and R7 and/or R8 and R9 can form a ring comprising from 3 to 8 atoms, which can bear substituents; with the proviso that R7 is different from R8 and when R7 is a tertbutyl radical R8 is not hydrogen; and (B) an alumoxane and/or a compound capable of forming an alkyl metallocene. 21. The catalyst according to claim 20 wherein in the metallocene compound of formula (T) G is a moiety of formula (Eta) or (IV) wherein said moieties are defined in claims 6 and 8, 22. The catalyst according to claim 21 wherein in the metallocene compound of formula (T) G is a moiety selected from the compound of formula (IVa) (IVb), (IVc) or (IVd) wherein said moieties are defined in claims 9-15. 23. The catalyst according to any of claims 20-22, wherein said alumoxane is methylalumoxane (MAO), isobutylalumoxane (TTBAO) and 2,4,4-trimethyl-pentylalumoxane (TTOAO). 24. The catalyst according to any of claims 20-22, wherein the compound capable of forming a metallocene alkyl cation is a compound of formula D^E", wherein D+ is a Bnansted acid, able to donate a proton and to react irreversibly with a substituesnt X of the metallocene of formula (I) and F is a compatible anion, which is able to stabilize the active catalytic species originating from the reaction of the two compounds, and which is sufficiently labile to be able to be removed by an olefinic monomer. 25. A process for the preparation of a polymer of alpha-olefins comprising contacting one or more alpha-olefins under polymerization conditions with a catalyst defined in any of claims 20-24. 26. The process according to claim 25 for the preparation of homo- and copolymers of propylene. 27. The process according to claim 26 wherein the process is carried out in the presence of an alpha-olefin selected from 1-butene, 1-pentene, 1-hexene, 4-metbyl-l-pentene, 1-octene, 1-decene and 1-dodecene. 28. The process according to claim 25 for the preparation of homo- and copolymers of ethylene. 29. The process according to claim 28, wherein the process is carried out in the presence of an olefin selected from propylene, 1-butene, 1-pentene, 4-methyl-l-pentene, 1-hexene, 1-octene, 4,6-dimethyl-l-heptene, 1-decene, 1-dodecene, 1-tetradecene, 1-hexadecene, 1-octadecene, 1-eicosene, allylcyclohexane, cyclopentene, cyclohexene and norbomene, 1,5-hexadiene, 1-6-heptadiene, 2-methyl-l,5-hexadiene, trans 1,4-hexadiene, cis 1,4- hexadiene, ' 6-methyl-l ,5-heptadiene, 3,7-dimethyM ,6-octadiene, 11 -methyl-1,10- dodecadiene, 5-ethylidene-2-norbornene. 30. The process according to any of claims 25-29 wherein the catalyst is supported on an inert carrier. 31. The process according to any of claims 25-30 characterized in that it is carried out in gas phase. |
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in-pct-2001-1314-che-abstract.pdf
in-pct-2001-1314-che-claims filed.pdf
in-pct-2001-1314-che-claims granted.pdf
in-pct-2001-1314-che-correspondnece-others.pdf
in-pct-2001-1314-che-correspondnece-po.pdf
in-pct-2001-1314-che-description complete filed.pdf
in-pct-2001-1314-che-description complete granted.pdf
in-pct-2001-1314-che-form 1.pdf
in-pct-2001-1314-che-form 19.pdf
in-pct-2001-1314-che-form 26.pdf
in-pct-2001-1314-che-form 3.pdf
in-pct-2001-1314-che-form 5.pdf
in-pct-2001-1314-che-other documents.pdf
| Patent Number | 212779 | |||||||||||||||
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| Indian Patent Application Number | IN/PCT/2001/1314/CHE | |||||||||||||||
| PG Journal Number | 07/2008 | |||||||||||||||
| Publication Date | 15-Feb-2008 | |||||||||||||||
| Grant Date | 17-Dec-2007 | |||||||||||||||
| Date of Filing | 21-Sep-2001 | |||||||||||||||
| Name of Patentee | BASELL TECHNOLOGY COMPANY B.V | |||||||||||||||
| Applicant Address | Hoeksteen 66 NL-2132 MS Hoofddorp | |||||||||||||||
Inventors:
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| PCT International Classification Number | C07F 17/00 | |||||||||||||||
| PCT International Application Number | PCT/EP2000/013191 | |||||||||||||||
| PCT International Filing date | 2000-12-22 | |||||||||||||||
PCT Conventions:
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