Abstract: A catalytic system based on at least one rare-earth metallocene and an organomagnesium reagent as co-catalyst of formula RB—(Mg—RA)m—Mg—RB is provided. According to the formula, RB comprises a benzene nucleus substituted with the magnesium atom. One of the carbon atoms of the benzene nucleus ortho to the magnesium is substituted with a methyl, an ethyl or an isopropyl or forms a ring with the carbon atom which is its closest neighbour and which is meta to the magnesium. The other carbon atom of the benzene nucleus ortho to the magnesium is substituted with a methyl, an ethyl or an isopropyl. RA is a divalent aliphatic hydrocarbon-based chain, optionally interrupted with one or more oxygen or sulfur atoms or with one or more arylene groups. The m is a number greater than or equal to 1, preferably 1. The catalytic system allows the synthesis of dienic and/or ethylenic telechelic polymers.

Abstract: A triblock polymer of formula B-A-B is provided. According to the formula, the symbol A represents a “central” block which is a statistical copolymer comprising units of a 1,3-diene and more than 50 mol % of ethylene units. The symbols B each represent an “end” block which is a polyethylene with a melting point of greater than 90° C. and a number-average molar mass of greater than or equal to 2000 g/mol and less than or equal to 10 000 g/mol. The polymer has improved rheological properties relative to a statistical copolymer based on ethylene and 1,3-diene of the same microstructure without changing its mechanical and dynamic or thermal properties.

Abstract: A process for preparing a multiblock polymer by statistical copolymerization of a mixture containing ethylene and a 1,3-diene and subsequent polymerization of ethylene in the presence of a rare-earth metallocene and an organomagnesium reagent RB—(Mg—RA)m—Mg—RB or X—Mg—RA—Mg—X is provided. According to the formula, RA is a divalent aliphatic hydrocarbon-based chain optionally interrupted with one or more oxygen or sulfur atoms or arylene groups, RB comprises a benzene nucleus substituted with the Mg atom, one of the carbon atoms of the benzene nucleus ortho to the Mg is substituted with a methyl, an ethyl or an isopropyl or forms a ring with the carbon atom which is its closest neighbour and which is meta to the Mg. The other carbon atom of the benzene nucleus ortho to the Mg is substituted with a methyl, ethyl or isopropyl, X being a halogen atom, m being greater than or equal to 1.

Abstract: A telechelic polymer of formula Z1-POLY-Z2 is provided. The term “POLY” denotes a polymer chain comprising units of a 1,3-diene, ethylene units and cyclic units, 1,2-cyclohexane units, Z1 and Z2 denoting a group containing a function, Z1 and Z2 being identical. The polymer has a macrostructure defined by a dispersity of less than 1.5 or by a number-average molar mass of greater than 10 000 g/mol.

Abstract: A catalytic system based on at least one rare-earth metallocene and as co-catalyst an organomagnesium reagent of formula X—Mg—RA—Mg—X is provided. In the formula, RA is a divalent aliphatic hydrocarbon-based chain, optionally interrupted with an oxygen atom, a sulfur atom or with an arylene group, and X is a halogen atom. The catalytic system allows the synthesis of dienic and/or ethylenic telechelic polymers.

Abstract: A process of producing a composition comprising a copolymer of ethylene and one or more C4-C8 ?-olefins, may include copolymerizing the ethylene and the one or more C4-C8 ?-olefins in the presence of a procatalyst and an alkylaluminum cocatalyst. The procatalyst may be a Ti-containing Ziegler Natta procatalyst and the polymerization may include the procatalyst and the alkylaluminum cocatalyst in amounts such that a molar ratio of Al:Ti ranges from about 0.5 to about 50.0.

Abstract: The present invention relates to a method for preparing a catalyst, and in particular provides a method for preparing a catalyst suitable for the polymerisation of ethylene and/or propylene, said catalyst comprising a compound of yttrium, neodymium or scandium supported on a silica support, and wherein the method comprises: a) Treating a silica support by heating at a temperature of at least 550° C., b) Contacting the treated silica support with a complex of the following formula: DmMX1X2R wherein M is selected from Y, Sc and Nd, R is a hydrocarbyl group, X1 and X2 are anionic groups, D is a neutral donor group, and m is 0 or greater.

Abstract: A diblock polymer composed of a first block and a second block is provided. The first block is a statistical copolymer comprising units of a 1,3-diene and more than 50 mol % of ethylene units. The second block is a polyethylene with a melting point above 90° C. and a number-average molar mass greater than or equal to 2000 g/mol and less than or equal to 10 000 g/mol. Such a diblock polymer has improved rheology compared to a statistical copolymer of the same microstructure and of the same macrostructure as the first block of the diblock polymer.

Abstract: An ethylene/1,3-butadiene copolymer containing ethylene units, butadiene units and UD units of cyclic, 1,2-cyclohexanediyl structure, and bearing, at one of its chain ends, an alkoxysilyl or silanol function, functional group F1 is provided.

Abstract: A copolymer of a 1,3-diene and of an olefin selected from the group consisting of ?-monoolefins, ethylene and mixtures thereof is provided. The copolymer bears, at one of its chain ends, an alkoxysilyl or silanol function, functional group F1, and the copolymer is different from a copolymer of a 1,3-diene and a vinylaromatic monomer.

Abstract: A process of producing a composition comprising a copolymer of ethylene and one or more C4-C8 ?-olefins, may include copolymerizing the ethylene and the one or more C4-C8 ?-olefins in the presence of a procatalyst and an alkylaluminum cocatalyst. The procatalyst may be a Ti-containing Ziegler Natta procatalyst and the polymerization may include the procatalyst and the alkylaluminum cocatalyst in amounts such that a molar ratio of Al:Ti ranges from about 0.5 to about 50.0.

Abstract: A copolymer comprising a copolymer chain A bearing a function B selected from the group consisting of the functions B1 and B2, the copolymer chain A being a copolymer chain comprising monomer units M1 and monomer units M2, M1 being a conjugated diene and M2 being a monomer selected from the group consisting of ?-monoolefins, ethylene and mixtures thereof, B1 being selected from the group consisting of N(SiMe3)2; N(SiMe2CH2CH2SiMe2); para-C6H4(NMe2); para-C6H4(OMe); para-C6H4(N(SiMe3)2); ortho-CH2-C6H4NMe2; ortho-CH2-C6H4OMe; C6F5; C3F7; C6F13; CH(OCH2CH2O); B2 being a function that is derived from B1, is provided. Such a copolymer is synthesized by using a transfer agent bearing the function B1 and a carbon-metal bond, the metal being an alkaline-earth metal, zinc or aluminium.

Abstract: A copolymer of a 1,3-diene and of an olefin selected from the group consisting of ?-monoolefins, ethylene and mixtures thereof is provided. The copolymer bears, at one of its chain ends, an alkoxysilyl or silanol function, functional group F1, and the copolymer is different from a copolymer of a 1,3-diene and a vinylaromatic monomer.

Abstract: An ethylene/1,3-butadiene copolymer containing ethylene units, butadiene units and UD units of cyclic, 1,2-cyclohexanediyl structure, and bearing, at one of its chain ends, an alkoxysilyl or silanol function, functional group F1 is provided.

Abstract: A compound and the use thereof to prepare a functional or telechelic polyolefin is provided. The compound has the following formula (II): Y((CH2)p—B?)m??(II), wherein m=2 or 3; Y being an alkaline earth metal or zinc when m=2, Y being aluminum when m=3; B? being selected from the group comprising N(SiMe3)2; N(SiMe2CH2CH2SiMe2); C6F5; C3F7; C6F13; para-C6H4—NMe2; para-C6H4—O-Me; para-C6H4—N(SiMe3)2; and CH(OCH2CH2O); and p being an integer from 0 to 50.

Abstract: A copolymer comprising a copolymer chain A bearing a function B selected from the group consisting of the functions B1 and B2, the copolymer chain A being a copolymer chain comprising monomer units M1 and monomer units M2, M1 being a conjugated diene and M2 being a monomer selected from the group consisting of ?-monoolefins, ethylene and mixtures thereof, B1 being selected from the group consisting of N(SiMe3)2; N(SiMe2CH2CH2SiMe2); para-C6H4(NMe2); para-C6H4(OMe); para-C6H4(N(SiMe3)2); ortho-CH2-C6H4NMe2; ortho-CH2-C6H4OMe; C6F5; C3F7; C6F13; CH(OCH2CH2O); B2 being a function that is derived from B1, is provided. Such a copolymer is synthesized by using a transfer agent bearing the function B1 and a carbon-metal bond, the metal being an alkaline-earth metal, zinc or aluminium.

Abstract: The invention herein pertains to a telechelic polyolefin of formula (III) or (IV) and to a process for its preparation, Z-A-(CH2)p—B???(III) Z-A-(CH2)p—B??(IV) A being a polymer chain obtained by homopolymerization of ethylene or by copolymerization of ethylene and an alpha-monoolefin; B? being selected from the group consisting of N(SiMe3)2; N(SiMe2CH2CH2SiMe2); para-C6H4(NMe2); para-C6H4(OMe); C6H4(N(SiMe3)2); ortho-CH2—C6H4NMe2; ortho-CH2—C6H4OMe; C6F5; C3F7; C6F13; CH(OCH2CH2O); B being the function B? or a function derived from B?; p being an integer from 0 to 50, advantageously from 0 to 11; Z being a function selected from the group consisting of halogens; thiols; thiol derivatives; azides; amines; alcohols; carboxylic acid function; isocyanates; silanes; phosphorus derivatives; dithioesters; dithiocarbamates; dithiocarbonates; trithiocarbonates; alkoxyamines; vinyl function; dienes; and the group -A-(CH2)p—B?.

Abstract: A compound and the use thereof to prepare a functional or telechelic polyolefin is provided. compound has the following formula (II): Y((CH2)p—B?)m ??(II), wherein m=2 or 3; Y being an alkaline earth metal or zinc when m=2, Y being aluminium when m=3; B? being selected from the group comprising N(SiMe3)2; N(SiMe2CH2CH2SiMe2); C6F5; C3F7; C6F13; para-C6H4—NMe2; para-C6H4—O-Me; para-C6H4—N(SiMe3)2; and CH(OCH2CH2O); and p being an integer from 0 to 50.

Abstract: Telechelic polyolefin of formula(I) and its derivatives: CH2?CH—(CH2)p-A-Z??(I) wherein: A represents a (co)polymer comprising at least 95 mol % of (CH2—CH2) units; Z is selected from the group comprising halogens, thiols and their derivatives, azides, amines, alcohols, the carboxylic acid function, isocyanates, silanes, phosphorous derivatives, dithioesters, dithiocarbamates, dithiocarbonates, trithiocarbonates, alkoxyamines, the vinyl function, dienes, and the group -A-(CH2)p—CH?CH2; p is a whole number between 1 and 20, most advantageously between 6 and 9.

Abstract: Activating supports may be suitably prepared by the following procedure (a) providing a porous mineral oxide support material, (b) treating the support with a phosphorus-containing compound, (c) treating the support from step (b) with an organometallic compound, (d) heating the functionalized support from step (c) under an inert gas and then under an atmosphere comprising oxygen, (e) fluorinating the support with a fluorinating agent, and (f) recovering an activating support. The activating supports are suitable used in combination with single site catalysts for the polymerization of olefins. The supports are most preferably used in combination with metallocene complexes. The preparative route for the activating supports provides for supported polymerization catalyst systems having excellent activities.