REACTION-MECHANISMS IN METALLOCENE-CATALYZED OLEFIN POLYMERIZATION

被引:3
作者
BRINTZINGER, H
BECK, S
LECLERC, M
STEHLING, U
ROLL, W
机构
[1] Fakultät für Chemie, Universität Konstanz
来源
CATALYST DESIGN FOR TAILOR-MADE POLYOLEFINS | 1994年 / 89卷
关键词
D O I
10.1016/S0167-2991(08)63034-7
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
1. Studies by H-1 NMR on equilibria between contact ion pairs such as Cp(2)ZrCH(3)(delta+)... H3C-B(C6F5)(3)(delta-) and binuclear alkyl zirconocene cations of the type (Cp(2)ZrCH(3))(2)(mu-CH3)(+) lead to the conclusion that these binuclear species must generally be considered as participants in all homogeneous Ziegler-Natta systems. 2. Different polypropene chain lengths, which are obtained from cis- and trans-1D - propene with the catalyst en(thind)(2)ZrCl2/MAO, show that exchange of alpha-H with alpha-D atoms affect the rate of chain growth by a large kinetic isotope effect; this supports the notion that an alpha-agostic interaction facilitates the olefin insertion step. 3. A strong increase in polymer chain lengths, which is caused by the presence of alpha-methyl groups in ansa-zirconocene catalysts, is shown, by the effects of propene pressure on M(w), to be due to the suppression of the otherwise predominant direct beta-H-transfer to a coordinated olefin molecule by these alpha-substituents.
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页码:193 / 200
页数:8
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