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可分离的平面正方形镍的β-氯代烷基配合物中β-氯消除的直接观察。

Direct observation of β-chloride elimination from an isolable β-chloroalkyl complex of square-planar nickel.

机构信息

Department of Chemistry and Biochemistry, University of California, San Diego , 9500 Gilman Drive, Mail Code 0358, La Jolla, California 92093-0358, United States.

出版信息

J Am Chem Soc. 2014 Nov 5;136(44):15481-4. doi: 10.1021/ja508956q. Epub 2014 Oct 21.

Abstract

Reported here are the isolation, structural characterization, and decomposition kinetics of the four-coordinate pentachloroethyl nickel complex, NiCl(CCl2CCl3)(CNAr(Mes2))2 (Ar(Mes2) = 2,6-(2,4,6-Me3C6H2)2C6H3). This complex is a unique example of a kinetically persistent β-chloroalkyl in a system relevant to coordination-insertion polymerization of polar olefins. Kinetic analysis of NiCl(CCl2CCl3)(CNAr(Mes2))2 decomposition indicates that β-chloride (β-Cl) elimination proceeds by a unimolecular mechanism that does not require initial dissociation of a CNAr(Mes2) ligand. The results suggest that a direct β-Cl elimination pathway is available to four-coordinate, Group 10 metal vinyl chloride polymerization systems.

摘要

报告了四配位五氯乙基镍配合物 NiCl(CCl2CCl3)(CNAr(Mes2))2 (Ar(Mes2) = 2,6-(2,4,6-Me3C6H2)2C6H3)的分离、结构表征和分解动力学。该配合物是与极性烯烃配位插入聚合相关的体系中动力学稳定的β-氯代烷基的独特实例。NiCl(CCl2CCl3)(CNAr(Mes2))2 分解的动力学分析表明,β-氯(β-Cl)消除通过不需要初始解离 CNAr(Mes2)配体的单分子机制进行。结果表明,四配位、第 10 族金属氯乙烯聚合体系存在直接的β-Cl 消除途径。

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