Combining oxidative addition and polymerization: A study towards the synthesis of macromonomers

W. Massa, N. Faza, Hak-Chul Kang, C. Focke, W. Heitz
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引用次数: 18

Abstract

Oxidative addition to a metal in a low valent state produces catalysts that allow reporter or functional groups to be introduced to a polymer chain end. Substituted allyltrifluoroacetates were added to Ni(0)(COD)2. The resulting π-allyl-Ni trifluoroacetates are dimeric in the solid state as well as in solution. The crystal structure of bis[(η3-2-phenylallyl)(trifluoroacetato)-nickel(II)], bis[(η3-2-trimethylsilylallyl)(trifluoroacetato)nickel(II)], are given and correlated with the reactivity as polymerization catalysts. Butadiene, styrene, and norbornene are used as monomers. The substituent of the allyl group is found quantitatively to be the end group of each macromolecule. Thus it is demonstrated that no chain transfer occurs.

氧化加成与聚合相结合:合成大单体的研究
对处于低价状态的金属进行氧化加成可以产生催化剂,使报告基团或官能团被引入到聚合物链的末端。将取代的烯丙基三氟乙酸盐加入到Ni(0)(COD)2中。所得的π-烯丙基-镍三氟乙酸酯在固体和溶液中均为二聚体。给出了双[(η - 3-2-苯丙烯基)(三氟乙酸)镍(II)]和双[(η - 3-2-三甲基硅丙烯基)(三氟乙酸)镍(II)]的晶体结构,并将其与聚合催化剂的反应活性进行了对比。丁二烯、苯乙烯和降冰片烯被用作单体。烯丙基的取代基被定量地发现是每个大分子的端基。因此,证明了不发生链转移。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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