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4699872 
Journal Article 
Synthesis of Ethylene or Propylene/1,3-Butadiene Copolymers Possessing Pendant Vinyl Groups with Virtually No Internal Olefins 
Michiue, K; Mitani, M; Fujita, T 
2015 
Catalysts
ISSN: 2073-4344 
2001-2017 
In general, ethylene/1,3-butadiene copolymerizations provides copolymers possessing both pendant vinyls and vinylenes as olefinic moieties. We, at MCI, studied the substituent effects of C-2-symmetric zirconocene complexes, rac-[Me2Si(Indenyl')(2)]ZrCl2 (Indenyl' = generic substituted indenyl), after activation on the ratio of the pendant vinyls and vinylenes of the resultant copolymers. Complexes examined in this study were rac-dimethylsilylbis(1-indenyl)zirconium dichloride (1), rac-dimethylsilyl-bis [1-(2-methyl-4,5-benzoindenyl)]zirconium dichloride (2), rac-dimethylsilyl-bis[l-(2-methyl-4-phenylindenyl)]zirconium dichloride (3), rac-dimethy1si1y1-bis(2-ethyl-4-phenylindenyl) zirconium dichloride (4), rac-dimethylsilyl-bis[l-(2-n-propyl -4-(1-naphthyl)indenyl)]zirconium dichloride (5), rac-dimethylsilyl-[1-(2-ethyl-4-(5-(2,2-dimethyl-2,3-dihydro-1H-cyclopenta [a]naphthalenyl)indenyl))][1-(2-n-propyl-4-(5-(2,2-dimethyl-2,3-dihydro-1H-cyclopenta[a] naphthalenyl)indenyl))]zirconium dichloride (6), rac-dimethylsilyl-bis[1-(2-ethyl -4-(9-phenanthryl)indenyl)]zirconium dichloride (7), and rac-dimethylsilyl-bis [l-(2-n-propyl-4-(9-phenanthryl)indenyl)]zirconium dichloride (8). We found that the ratio of the pendant vinyls and vinylenes is strongly affected by the bulkiness of the substituent on the complexes examined. The vinyl content increased linearly in the following order, 8 > 7 > 6 > 5 > 4 > 3 > 2 > 1. Notably, complex 8/DMAO formed ethylene/1,3-butadiene copolymers possessing predominant vinyl groups, which can be crucial precursors for functionalized polyolefins. Likewise, complex 8/DMAO afforded propylene/1,3-butadiene copolymers with predominant vinyl groups. 
1,3-butadiene; C-2-symmetric zirconocene; insertion mode; vinyl groups; internal olefins; vinylenes