Abstract: A method for preparing tyrosine derived polyarylates includes combining a desaminotyrosyl-tyrosine ethyl ester, a desaminotyrosyl-tyrosine benzylester, succinic acid and a catalyst in a flask to produce a first mixture. Methylene chloride is added to the first mixture to produce a first suspension. Diisopropylcarbodiimide (DIPC) is added to the first mixture to produce a first solution. The first solution is added to a non-solvent to produce a precipitate. The precipitate is dissolved in methylene chloride to form a polymer solution. The polymer solution is blended with a slurry to produce polymer shreds. The polymer shreds are blended with a second slurry to produce a tyrosine derived polyarylate.

Abstract: [Object] There is provided a method which enables an olefin polymer having high melting point and high molecular weight to be produced even at high temperature proper in an industrial production process. [Solution] A method for producing an olefin polymer is provided, the method including polymerizing an olefin having two or more carbon atoms in the presence of a catalyst for olefin polymerization, wherein the catalyst for olefin polymerization includes (A) a bridged metallocene compound represented by Formula [1] and (B) at least one compound selected from, for example, an organoaluminum oxy-compound and an organoaluminum compound: [where R1 to R4 each represent, for example, a hydrocarbon group; R5 to R9 each represent, for example, a hydrogen atom or a halogen atom; R10 and R11 each represent, for example, a hydrogen atom; and R12 represents, for example, a hydrocarbon group. Y represents, for example, a carbon atom.

Abstract: In general the present invention provides a process for forming conjugated diene polymer, the process comprising the step of polymerizing conjugated diene monomer in the presence of a catalytically effective amount of a catalyst composition formed by combining (a) a nickel-containing compound, (b) an alkylating agent, (c) a fluorine-containing compound, (d) a carboxylic acid, and (e) an alcohol.

Abstract: Catalyst component for the polymerization of olefins CH2?CHR in which R is hydrogen or a hydrocarbyl radical with 1-12 carbon atoms, comprising Mg, Ti, halogen and two electron donor compounds one of which selected from alkoxybenzenes and the other being selected from those of formula (II) where RI and RII are the same or different and are hydrogen or linear or branched C1-C18 hydrocarbon groups which can also form one or more cyclic structures; RIII groups, equal or different from each other, are hydrogen or C1-C18 hydrocarbon groups; RIV groups equal or different from each other, have the same meaning of RIII except that they cannot be hydrogen; each of RI to RIV groups can contain heteroatoms selected from halogens, N, O, S and Si.

Abstract: The invention is directed to a metallocene catalyst system and a process for preparing the system. The metallocene catalyst system comprises a support and metallocene bound substantially throughout the support. The selection of certain supports facilitates the production of metallocene catalyst systems having increased catalytic activity than previously recognized.

Abstract: Methods for controlling properties of an olefin polymer using an organozinc compound are disclosed. The HLMI/MI shear ratio of the polymer can be decreased and the Mz/Mw ratio of the polymer can be increased via the addition of the organozinc compound.

Abstract: Process for the preparation of polybutadiene effected by the polymerization of butadiene in an aliphatic and/or cyclo-aliphatic solvent in the presence of a catalytic system prepared in situ which comprises: (i) a carboxylate of neodymium soluble in the process solvent containing a variable quantity of water, the H2O/Nd molar ratio ranging from 0.001/1 to 0.50/1; (ii) an alkyl compound of aluminum; (iii) an alkyl compound of aluminum in which at least one bond of Al consists of an Al—Cl bond; The total Al/Nd molar ratio ranging from 4/1 to 12/1, and the Cl/Nd molar ratio ranging from 2/1 to 6/1.

Abstract: The present invention discloses catalyst compositions employing transition metal complexes with a thiolate ligand. Methods for making these transition metal complexes and for using such compounds in catalyst compositions for the polymerization of olefins also are provided.

Abstract: The invention relates to A process for the polymerization of ethylene to produce a polyethylene resin in at least two slurry loop reactors connected to each other in series, the resin having a bimodal molecular weight distribution, a molecular weight distribution MWD of at least 7.0, an HLMI of from 1 to 100 g/10 min, and a density of from 0.935 to 0.960 g/cm3, wherein in one reactor 30 to 47 wt % based on the total weight of the polyethylene resin of a high molecular weight (HMW) polyethylene fraction is produced having an HL275 of from 0.05 to 1.8 g/10 min (the equivalent of HLMI of from 0.01 to 1.56 g/10 min), a density of from 0.925 to 0.942 g/cm3 and an MWD of at least 5.0, and in the other reactor a low molecular weight (LMW) polyethylene fraction is produced having an HLMI of from 10 to 1500 g/10 min and a density of from 0.960 to 0.975 g/cm3, in the presence of a Ziegler-Natta catalyst system.

Abstract: Methods for gas phase olefin polymerization are provided. The method can include combining a spray dried catalyst system with a diluent to produce a catalyst slurry. The catalyst system can include a metallocene compound. Ethylene, a continuity additive, and the catalyst slurry can be introduced to a gas phase fluidized bed reactor. The reactor can be operated at conditions sufficient to produce a polyethylene. The spray dried catalyst system can have a catalyst productivity of at least 12,000 grams polyethylene per gram of the catalyst system.

Abstract: The invention is directed to a metallocene catalyst system comprising an inert silica support having pores with a peak pore volume of greater than about 0.115 mL/g at a pore diameter between about 250 Angstroms and about 350 Angstroms, and an alumoxane activator, with the metallocene being bound substantially throughout the support. The activator is grafted to the support in a solvent at a reflux temperature of toluene to obtain an aluminoxane on silica, and a metallocene component is added to make a MCS having a metallocene loading of about 2 wt %. This facilitates the production of metallocene catalyst systems having increased catalytic activity than previously recognized that is at least about 20 percent higher than the catalytic activity for a metallocene loading of about 1 wt % where the activator is grafted to the support at room temperature.

Abstract: Catalyst component for the polymerization of olefins CH2?CHR in which R is hydrogen or a hydrocarbyl radical with 1-12 carbon atoms, comprising Mg, Ti, halogen and two electron donor compounds one of which selected from alkoxybenzenes and the other being selected from those of formula (II) where RI and RII are the same or different and are hydrogen or linear or branched C1-C18 hydrocarbon groups which can also form one or more cyclic structures; RIII groups, equal or different from each other, are hydrogen or C1-C18 hydrocarbon groups; RIV groups equal or different from each other, have the same meaning of RIII except that they cannot be hydrogen; each of RI to RIV groups can contain heteroatoms selected from halogens, N, O, S and Si.

Abstract: A production process of a contact product, which can be used as a polymerization catalyst component, comprising contacting a metal oxide such as zinc oxide with a compound defined by a specific formula such as trifluoroacetic acid; a production process of a polymerization catalyst, comprising contacting the polymerization catalyst component with a transition metal compound; and a production process of a polymer, comprising polymerizing an addition-polymerizable monomer in the presence of the polymerization catalyst.

Abstract: The invention relates to a high-molecular-weight, linear, neodymium-catalysed polybutadiene having a high proportion, >95%, of cis-1,4 units having a low proportion, <1%, of 1,2-vinyl content, and also having a small molar-mass-polydispersity index (MPI), characterized in that Mooney viscosity (ML1+4100° C.) of the polybutadiene is from 70 to 90 and The molar-mass-polydispersity index of the polybutadiene is smaller than 10.

Abstract: A production process of a contact product, which can be used as a polymerization catalyst component, comprising contacting a compound defined by a specific formula, such as diethyl zinc, with a compound defined by a specific formula, such as pentafluorobutyric acid; a production process of a polymerization catalyst, comprising contacting the polymerization catalyst component with a transition metal compound; and a production process of a polymer, comprising polymerizing an addition-polymerizable monomer in the presence of the polymerization catalyst.

Abstract: Catalyst compositions, methods of forming the same and polymers formed therefrom are described herein.

Abstract: The present invention provides a polymerization process which is conducted by contacting an olefin monomer and at least one olefin comonomer in the presence of hydrogen and a metallocene-based catalyst composition. Polymers produced from the polymerization process are also provided, and these polymers have a reverse comonomer distribution, low levels of long chain branches, and a ratio of Mw/Mn from about 3 to about 6.

Abstract: The invention concerns a novel catalytic combination for polymerizing alpha-olefins based on a titanium diamidide complex. The invention also concerns a method for polymerizing alpha-olefins using said catalytic combination, in the absence of any aluminum-containing compound. The inventive catalytic combination comprises: component A which is a dichlorinated titanium diamidide complex of general formula (I) wherein R represents a methyl group (component A2) or an isopropyl group (component A1); component B which is a dialkylmagnesium whereof the reaction with component A enables an alkylated component AA to be obtained: and as activator of said component AA, component C which is trispentafluorophenylboran (B(C6F5)3).

Abstract: Disclosed is a homogeneous catalyst system for producing an ethylene homopolymer or an ethylene copolymer with ?-olefin. Specifically, this invention pertains to a transition metal catalyst which has stability under high temperature solution polymerization at 120˜250° C., in which a cyclopentadiene derivative and an electron donating substituent, both of which are bonded to a Group IV transition metal acting as a central metal, are crosslinked through a silyl derivative substituted with a cyclohexyl, to a catalyst system including such a transition metal catalyst and an aluminoxane cocatalyst or a boron compound cocatalyst, and to a method of producing an ethylene homopolymer or an ethylene copolymer with ?-olefin, having high molecular weight, using the catalyst system under conditions of high-temperature solution polymerization.

Abstract: A process for producing an olefin polymerization catalyst, comprising steps of (1) contacting a defined amount of a zinc compound represented by the defined formula, Zn(L1)2, with a defined amount of a halogenated alcohol represented by the defined formula, R1R2R3C—OH, thereby forming a zinc atom-containing compound, and (2) contacting the zinc atom-containing compound, a solid catalyst component containing a titanium atom, a magnesium atom and a halogen atom, an organoaluminum compound, and an external electron donor with one another; and a production process of an olefin polymer, comprising a step of polymerizing an olefin in the presence of an olefin polymerization catalyst produced by the above process.

Abstract: The invention refers to a process for preparing a Group 2 metal/transition metal olefin polymerization catalyst component in particulate form having improved polymerization properties due to the use of H2 during catalyst component preparation and the use of such catalyst components in a process for polymerizing olefins.

Abstract: Disclosed is a bimodal Ziegler-Natta catalyzed polyethylene, having a density of from 0.930 g/cc to 0.960 g/cc, and a molecular weight distribution of from 10 to 25, wherein an article formed therefrom has a PENT of at least 1500. Also disclosed is a method of preparing a tubular article including obtaining a bimodal polyethylene having a density of from 0.930 g/cc to 0.960 g/cc and a molecular weight distribution of from 10 to 25, and processing the polyethylene under conditions where a specific energy input (SEI) is less than 300 kW·h/ton, and wherein the article has a PENT of at least 1500. Further disclosed is a method for controlling the degradation of polyethylene including polymerizing ethylene monomer, recovering polyethylene, extruding the polyethylene, and controlling the degradation of polyethylene by measuring the SEI to the extruder and adjusting throughput and/or gear suction pressure keep SEI less than 300 kW·h/ton, and forming an article.

Abstract: A catalyst composition for polymerizing olefins to polymers having bimodal molecular weight distribution comprises two transition metal-containing metallocene compounds, a magnesium compound, an alcohol, an aluminum containing co-catalyst and a polymeric support. The transition metal in one of the metallocene compounds is zirconium and the transition metal in the second metallocene compound is selected from the group consisting of titanium, vanadium and hafnium. Polyolefin polymers made using the catalyst composition have broad molecular weight distributions and are useful in film and blow molding applications.

Abstract: The present invention provides a method of polymerization of olefin or copolymerization of olefin/alpha-olefin using transition metal compound with an oxidation number of 3 as a catalyst and organo-aluminum compound as a co-catalyst, wherein the transition metal compound with an oxidation number of 3 is produced by reacting organo-magnesium compound with a compound which is formed by reacting transition metal compound having aryloxy group with an oxidation number of 4 or more with external electron donor. According to the present invention, an olefin (co)polymer with a narrow molecular weight distribution is obtained.

Abstract: The invention relates to the use of nitrogenous aluminium organyl complexes of general formula (I) as co-catalysts in heterogeneous polymerisation reactions of propene. In said formula: R, R?, R1 and R1? independently of one another represent branched or unbranched C1-C7 alkyl, cycloalkyl, alkenyl, cycloalkenyl, aryl or alkynyl; R2 represents unsubstituted, monoalkylated or polyalkylated and/or monofluorinated or polyfluorinated aromatic hydrocarbons from group (II); R3 and R4 independently of one another represent CH2, CF2 oder C(R1)2; m stands for 0, 1 or 2; n stands for 0, 1 or 2; o stands for 0 or 1, all independently of one another.

Abstract: A modified particle obtained by a process containing contacting a Bi compound, a compound having an electron-withdrawing group and an active hydrogen and particle; and a catalyst component for addition polymerization containing the modified particle; a catalyst for addition polymerization prepared by a process containing contacting the modified particle (A) and a transition metal compound of Groups 3 to 11 or lantanide series (B); and a catalyst for addition polymerization prepared by a process containing contacting the modified particle (A) and a transition metal compound of Groups 3 to 11 or lantanide series (B) and an orbanoaluminum compound (C); and a process for producing an addition polymer with the catalyst.

Abstract: A catalyst component for ethylene polymerization, including an inorganic oxide support, and at least one alkyl metal compound, at least one halide, at least one dihydrocarbyl magnesium compound, at least one difunctional compound that reacts with the dihydrocarbyl magnesium compound and at least one titanium compound, wherein the difunctional compound is a mono-, di- or multi-halogenated alcohol or phenol having from 2 to 20 carbon atoms; or a mono-, di- or multi-halogenated acyl halide having from 2 to 20 carbon atoms. Also, a process for preparing the catalyst component and use thereof.

Abstract: A process for polymerizing an olefin is capable of polymerizing an olefin with excellent polymerization activity, and comprises polymerizing or copolymerizing an olefin at a polymerization reaction temperature of 50 to 200° C. in the presence of a catalyst comprising a transition metal compound (A) represented by the following formula (I), a compound (B-1) having a reduction ability which reacts with the transition metal compound (A) to convert an imine structure moiety to a metal amide structure, and a compound (B-2) which reacts with the transition metal compound (A) to form an ion pair; wherein M is a transition metal atom of Groups 3 to 11 of the periodic table; m is an integer of 1 to 6; Y is O, S, Se, or —C(R7)—; R1 to R7 may be the same or different, and are each a hydrogen atom, a halogen atom, a hydrocarbon group, an oxgen-containing group, a nitrogen-containing group and the like; n is a number satisfying a valence of M; and X is a hydrogen atom, a halogen atom, a hydrocarbon group and the like.

Abstract: A method for preparing a supported organometallic complex is disclosed. An organometallic complex is combined with a support material that has been treated with an organozinc compound. The organometallic complex comprises a Group 3 to 10 transition metal and an indenoindolyl ligand that is bonded to the transition metal. Also disclosed is a process for polymerizing an olefin using the supported complex. Organozinc treatment of the support unexpectedly boosts catalyst activity and polyolefin molecular weight.

Abstract: The present invention relates to a method for the prepolymerization of ?-olefin in the presence of a catalyst system which comprises (a) a magnesium supported solid complex titanium catalyst and (b) an organometallic compound of metal of Group I or III of the Periodic Table, characterized in that an inert solvent having high viscosity with molecular weight of 300 g/mole or more is used as a reaction medium.

Abstract: A catalyst obtained by contacting a specific transition metal compound (A) of Group 7 of the Periodic Table of the Elements, having a pyrazolyl group with an aluminum compound selected from organoaluminums and aluminoxanes and/or a specific boron compound, and a process for producing an addition polymer which comprises polymerizing an addition polymerizable monomer with the catalyst.

Abstract: A catalyst for addition polymerization obtained by bringing the following (A) into contact with (B) a specific organic aluminum compound and/or aluminoxane, and (C) a specific boron compound, and a process for producing an addition polymer with the same.

Abstract: The invention relates to a process for the preparation of an olefin polymerisation catalyst component, said catalyst component and its use. The process is mainly characterized by the steps of (i) reacting in solution a magnesium compound containing an alkoxy group, a carboxylic acid halide and a four-valent titanium compound containing a halogen, for obtaining a dissolved reaction product and (ii) recovering a fraction of the reaction product from step (i) in particulate form by contacting the dissolved reaction product with a mixture of an aromatic and an aliphatic hydrocarbon, or by contacting the dissolved reaction product first with an aromatic hydrocarbon and then with an aliphatic hydrocarbon, the amount of aromatic and aliphatic hydrocarbon being at least 5 mol per mol of magnesium.

Abstract: Provided are catalysts for styrene polymerization capable of efficiently and inexpensively producing styrenic polymers having a syndiotactic structure; and a method for producing styrenic polymers. The catalysts comprise (A) a transition metal compound, (B) an oxygen-containing compound and/or a compound capable of reacting with a transition metal compound to form an ionic complex, (C) a specific metal compound, preferably a specific organoaluminium compound of a general formula: ((R1)3—CO)n-Al—(R2)3−n wherein R1 represents an aliphatic hydrocarbon group having from 1 to 30 carbon atoms, an aromatic hydrocarbon group having from 6 to 30 carbon atoms or the like; R2 represents a hydrocarbon group; n is 1 or 2, and optionally (D) an alkylating agent. In the method for producing styrenic polymers, used is the catalyst.

Abstract: The present invention includes polymerization catalyst activator complexes which include at least Group 13 metals. The activator complexes of the invention are prepared, in general, by reacting a halogenated aryl Group 13 metal compound with a diol. The activator compound is represented in one aspect by: wherein each M1 is a Group 13 atom; each R3, R3′, R3″, and R3′″ group is independently selected from, for example, C1 to C30 alkyls, halogenated C1 to C30 alkyls, C6 to C60 halogenated aryls; with the proviso that at least one of R3, R3′, R3″, and R3′″ is a fluorinated C6 to C60 aryl group; R1 and R2 are independently selected from substituted or unsubstituted C1 to C100 hydrocarbylenes; R, when present, is a substituted or unsubstituted C30 hydrocarbylene; wherein when R is absent, R1 and R2 are bound together; and x is 0 or an integer from 1 to 100.

Abstract: A process for producing a polymer, which comprises polymerizing a vinyl compound (I) represented by the general formula CH2═CH—R, wherein steric parameters Es and B1 of the substituent R are respectively −1.64 or less and 1.53 or more, or a vinyl compound (II) represented by the general formula CH2═CH—R′, wherein a substituent R′ is a secondary or tertiary alkyl group, in the presence of a catalyst obtained by combining: (A) a transition metal compound represented by the general formula [1] (B) an organoaluminum compound and (C) a boron compound.

Abstract: Disclosed is a novel bidentate pyridine transition metal catalyst having the general formula 1

Abstract: Catalyst system for the polymerization of olefins CH2═CHR, wherein R is hydrogen or a hydrocarbon radical having 1-12 carbon atoms, comprising the product of the reaction between (a) a solid catalyst component comprising Mg, Ti, and halogen, (b) dimethylaluminium chloride (DMAC) and (c) an alkylaluinium compound, in which the molar ratio between (b) and (c) is lower than 10. This kind of catalyst system is particularly suitable for the preparation of copolymers of ethylene with &agr;-olefins due to its high capacity for incorporating the comonomer while at the same time maintaining high yields.

Abstract: Ethylene copolymers are prepared with comonomers selected from: (a) &agr;-olefins, (b) cycloolefins and (c) polyenes, with a content of ethylene units of between 80 and 99 mol %, a content of units derived from &agr;-olefin, cycloolefin and/or polyene comonomers of between 1 and 20 mol %, characterized in that: (a) in TREF (Temperature Rising Elution Fractionation) analysis, a quantity equal to at least 90% by weight of the copolymer is eluted within a temperature interval of less than 50° C., and (b) Mw/Mn>3, where Mw is the weight-average molecular weight and Mn is the number-average molecular weight, both determined by means of GPC.

Abstract: A process for production of an olefin polymer is provided which comprises polymerization of ethylene and/or &agr;-olefin of three of more carbons at a polymerization temperature of not lower than 120° C. with a catalyst comprising a specific metallocene compound having a substituted fluorenyl group, and a compound which reacts with the metallocene compound to form a cationic metallocene compound. The olefin polymer or copolymer produced by the process has narrow composition distribution, narrow molecular weight distribution, and a high molecular weight.

Abstract: The present invention relates to a catalyst for polymerization of olefin and the method of polymerization using the same, or more particularly, to a new catalyst for polymerization of olefin of a hybrid concept and the method of polymerization using the same, which comprises synthesizing a titanium compound chelated by means of amide and cyclopentadiene-based ligands, and activating the same by means of conventional MgCl2, etc., instead of using expensive methylaluminoxane. Moreover, the present invention can produce polymers of narrow distribution of molecular weights and even distribution of composition of co-polymers.

Abstract: An ethylene polymerization process is disclosed. The polyethylene has a long-chain-branching index (LCBI) of 1 or greaster. The process uses a single-site catalyst that contains a boraaryl ligand. The catalyst is alkylated with triisobutyl aluminum.

Abstract: A catalyst system which can be used in the polymerization of propylene comprises at least one metallocene as a rac/meso isomer mixture, at least one organoboroaluminum compound, at least one passivated support, at least one Lewis base and, if desired, at least one further organometallic compound.

Abstract: A polymerization process for the preparation of vinylic polymers from the corresponding vinylic monomers which process comprises the step of reacting a vinylic monomer in the presence of a catalyst system comprising a) a compound of general formula (I) where M is any metal capable of coordinating to an enolate or delocalized enolate-like species; B1, B2, B3 and B4 are chosen from nitrogen, oxygen, sulphur or phosphorus containing moieties wherein each of said nitrogen, oxygen, sulphur or phosporus is linked to at least one carbon atom of an organic group and to M; X1 is selected from the group consisting of alkyl, H, halogen, alkoxy, thiol aryloxy, ester, b) a metal, complex of general formula (II) where A is selected from the group consisting of nickel, iron, cobalt, chromium, manganese, titanium, zirconium, vanadium and the rare earth metals; L1, L2, L3 and L4 are ligands and c) a Lewis acid of general formula (III) wherein at least one of W, Y or Z is capable of forming a co-ordination bond with A and the

Abstract: Described are catalyst systems having aluminium alkyl complexes of the formula (I) described herein applied to magnesium chloride, SiO2 or SiO2 in combination with MgCl2 as support in the presence of titanium halides or vanadium halides and internal and, if desired, external donors act both as cocatalysts and as stereoselectivity promoters in heterogeneous polymerizations of &agr;-olefins. Also described are polymerization methods using these catalyst systems.

Abstract: Modified polybutadiene having a high-cis and low-trans structure with a moderate 1,2-structure content and exhibiting improved characteristics such as cold flow properties, which is obtained by modifying starting polybutadiene having a Tcp/ML1+4 ratio (Tcp: 5% toluene solution viscosity at 25° C.ML1+4: Mooney viscosity at 100° C.) of 2.5 or more in the presence of a transition metal catalyst.

Abstract: The present invention provides a method for varying the melting points and molecular weights of polyolefins by changing the structure of the catalyst used in the polymerization. The catalysts that are useful in the present invention are chiral, stereorigid metallocene catalyst of the formula R″(C5R″m)2MeQ. The catalysts include a bridge structure between the (C5R′m) groups and may contain substituents on the groups. It has been discovered that the melting points and molecular weights of the polymers produced by such catalysts are influenced by the bridge and substituents added to the (C5R′m) groups. Thus, the present invention provides a method for varying the melting points of the polymer product and a method of varying the molecular weights of the product by changing the components and structure of the metallocene catalysts. The present invention also provides a process for polymerizing olefins in which the melting points and/or molecular weights of the product may be controlled.

Abstract: A process for producing a styrenic copolymer having a functional group and a syndiotactic configuration is provided. The process comprises bringing a metal compound into interaction with a vinyl compound having a functional group to mask the functional group and copolymerizing the vinyl compound having the masked functional group with a styrenic compound in the presence of a polymerization catalyst comprising (A) a transition metal compound, (B) at least one compound selected from compounds having oxygen and compounds which can form ionic complex compounds by reaction with the transition metal compound and (C) an organometallic compound. A styrenic copolymer which is a random, block or graft copolymer, preferably a random copolymer, of a vinyl compound having a functional group and a styrenic compound and has the repeating units derived from the styrenic compound having the syndiotactic configuration can be produced efficiently.

Abstract: A process for producing a styrenic copolymer having a functional group and the syndiotactic configuration is provided. The process comprises bringing a metal compound into interaction with a vinyl compound having a functional group to mask the functional group and copolymerizing the vinyl compound having the masked functional group with a styrenic compound in the presence of a polymerization catalyst comprising (A) a transition metal compound, (B) at least one compound selected from compounds having oxygen and compounds which can form ionic complex compounds by reaction with the transition metal compound and (C) an organometallic compound. A styrenic copolymer which is a random, block or graft copolymer, preferably a random copolymer, of a vinyl compound having a functional group and a styrenic compound and has the repeating units derived from the styrenic compound having the syndiotactic configuration can be produced efficiently.

Abstract: The present invention relates to a catalyst system comprising metallocene, cocatalyst, support material and, if desired, further organometallic compounds. The catalyst system can advantageously be used for the polymerization of olefins, where the use of aluminoxanes such as methylaluminoxane (MAO), which usually has to be used in a large excess, as cocatalyst can be dispensed with and a high catalyst activity and good polymer morphology are nevertheless achieved.