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N-(5,6,7-三氢喹啉-8-亚基)-2-二苯甲酮苯亚胺镍卤化物配合物的合成、表征及其对乙烯聚合的催化行为。

N-(5,6,7-trihydroquinolin-8-ylidene)-2-benzhydrylbenzenaminonickel halide complexes: synthesis, characterization and catalytic behavior towards ethylene polymerization.

机构信息

School of Chemistry and Chemical Engineering, Shanxi University, Taiyuan, 030006, China.

出版信息

Dalton Trans. 2012 Feb 7;41(5):1617-23. doi: 10.1039/c1dt11766a. Epub 2011 Dec 8.

Abstract

A series of N-(5,6,7-trihydroquinolinylidene)-2-benzhydrylbenzenamine ligands was synthesized and characterized by (1)H/(13)C NMR and IR spectroscopy, and by elemental analysis. These ligands reacted with NiCl(2) or NiBr(2)(DME) to form the title halide complexes, which were also characterized by IR spectroscopy and elemental analysis. Single crystal X-ray diffraction revealed that the representative nickel complexes crystallized as centro-symmetric dimers with chloro-bridges linking distorted octahedral nickel centers. On activation with either methylaluminoxane (MAO) or diethylaluminium chloride (Et(2)AlCl), all nickel pre-catalysts showed high activities for ethylene polymerization, producing polyethylene with narrow molecular weight distribution, consistent with single-site catalysis. The nature of the ligands and reaction parameters were investigated and discussed in terms of their influence on the catalytic behavior of these nickel pre-catalysts.

摘要

一系列 N-(5,6,7-三氢喹啉亚基)-2-二苯甲基苯胺配体通过 1H/13C NMR 和 IR 光谱以及元素分析进行了合成和表征。这些配体与 NiCl2 或 NiBr2(DME)反应形成标题卤化物配合物,这些配合物也通过 IR 光谱和元素分析进行了表征。单晶 X 射线衍射表明,代表性的镍配合物结晶为中心对称二聚体,氯桥连接扭曲的八面体镍中心。用甲基铝氧烷 (MAO) 或二乙基氯化铝 (Et2AlCl) 活化后,所有镍前催化剂对乙烯聚合表现出高活性,生成分子量分布较窄的聚乙烯,与单活性位催化一致。考察了配体的性质和反应参数,并讨论了它们对这些镍前催化剂催化行为的影响。

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