Copolymerization of ethylene with alpha-olefin catalyzed by [1,8-C10H6((NSiBuMe2)-Bu-t)(2)]TiCl2 and [ArN(CH2)(3)NAr]TiCl2 (Ar=2, 6-(Pr2C6H3)-Pr-i)-MMAO catalyst systems

Citation
K. Nomura et al., Copolymerization of ethylene with alpha-olefin catalyzed by [1,8-C10H6((NSiBuMe2)-Bu-t)(2)]TiCl2 and [ArN(CH2)(3)NAr]TiCl2 (Ar=2, 6-(Pr2C6H3)-Pr-i)-MMAO catalyst systems, POLYMER, 41(8), 2000, pp. 2755-2764
Citations number
60
Categorie Soggetti
Organic Chemistry/Polymer Science
Journal title
POLYMER
ISSN journal
00323861 → ACNP
Volume
41
Issue
8
Year of publication
2000
Pages
2755 - 2764
Database
ISI
SICI code
0032-3861(200004)41:8<2755:COEWAC>2.0.ZU;2-Z
Abstract
Copolymerization of ethylene with 1-hexene, 1-octene and 1-decene catalyzed by [1.8-C10H6(NR)(2)]TiCl2 [R = (SiBuMe2)-Bu-t (1)] and [ArN(CH2)(3)NAr]Ti Cl2 [Ar = 2,6-(Pr2C6H3)-Pr-i (2)] complexes-MMAO (MMAO = methyl isobutyl al uminoxane) catalyst systems have been explored. It was revealed that alpha- olefin contents in the resultant copolymer are highly dependent upon cataly st complex used. The resultant copolymer with 1 gave relatively broad molec ular weight distributions, consisting of high and low molecular weight copo lymers. On the other hand, it was difficult to prepare high molecular weigh t (M-w > 100, 000) copolymer with low alpha-olefin content if complex 2 was employed as the catalyst component. The resultant copolymers prepared by b oth 1 and 2 have been analyzed by DSC, C-13 NMR, and CFC (cross-fractionati on chromatography). The design of catalyst structure as well as ligands is thus necessary to prepare the desired ethylene/alpha-olefin copolymers by n on-metallocene type catalyst. (C) 2000 Elsevier Science Ltd. All rights res erved.