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首页> 外文期刊>Organometallics >Elemental reactions in copolymerization of α-olefins by bis(cyclopentadienyl) zirconocene and hafnocene: Effects of the metal as a function of the monomer and the chain end
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Elemental reactions in copolymerization of α-olefins by bis(cyclopentadienyl) zirconocene and hafnocene: Effects of the metal as a function of the monomer and the chain end

机译:双(环戊二烯)锆茂与ha茂共聚α-烯烃共聚合中的元素反应:金属对单体和链端的影响

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摘要

The effect of the metal on elementary chain propagation and termination reactions in hafnocene- and zirconocene-catalyzed olefin copolymerization processes has been systematically studied by quantum chemical methods. Two consecutive monomer insertions, parallel with the competing chain termination reactions, were studied for copolymerization of ethene with propene, 1-butene, and 1-hexene. For the purpose of a comparative study, analogous species along the reaction pathway were studied for each metallocene/monomer combination. Effects due to incorporation of a comonomer were analyzed as a function of both the central metal and the comonomer size. In accordance with the general experimental observations of zirconocenes producing lower molecular weight polymer than the hafnocenes, differences in activation energies for chain propagation and termination are smaller for the zirconocene. For the zirconocene, the activation energy is particularly low for β-hydrogen elimination after secondary comonomer insertion.
机译:已经通过量子化学方法系统地研究了金属对ha茂和锆茂催化的烯烃共聚过程中元素链增长和终止反应的影响。研究了两个连续的单体插入,与竞争性链终止反应平行,研究了乙烯与丙烯,1-丁烯和1-己烯的共聚。为了进行比较研究,研究了每种茂金属/单体组合沿反应路径的类似物种。分析了由于掺入共聚单体引起的影响,该影响是中心金属和共聚单体尺寸的函数。根据锆茂制备的分子量低于the烯的分子量更高的聚合物的一般实验观察结果,锆茂的链扩展和终止活化能的差异较小。对于锆茂,在二次共聚单体插入后,用于消除β-氢的活化能特别低。

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