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远程取代NHC配体中的铁和钴金属otropy:金属化生成异常NHC配合物或NHC开环

Iron and Cobalt Metallotropism in Remote-Substituted NHC Ligands: Metalation to Abnormal NHC Complexes or NHC Ring Opening.

作者信息

Danopoulos Andreas A, Massard Alexandre, Frison Gilles, Braunstein Pierre

机构信息

Université de Strasbourg, CNRS, Chimie UMR 7177, Laboratoire de Chimie de Coordination, 4 rue Blaise Pascal, 67081, Strasbourg Cedex, France.

Chemistry Department, National and Kapodistrian University of Athens, Panepistimiopolis Zografou, 15771, Athens, Greece.

出版信息

Angew Chem Int Ed Engl. 2018 Oct 26;57(44):14550-14554. doi: 10.1002/anie.201808008. Epub 2018 Sep 19.

Abstract

Metallotropism of the M[N(SiMe ) ] metal fragment in the tautomeric system IA ⇌AC involving imidazolium salts/N-heterocyclic carbenes with remote aminide/amine substituents, respectively, is manifested by its C carbophilicity (R=tBu, M=Co, Fe) or NR nitrogenophilicity (R=Cy, M=Co, Fe; R=Mes, M=Fe) and has been rationalized on the basis of steric and electronic effects. The thermolysis products of the [M{N(SiMe ) } ]/ IA ⇌AC system are also substituent-dependent, leading to a rearranged aminide-functionalized aNHC Co complex of an unprecedented type or to ring-opened metallaketenimines; they are postulated to originate from different metalloisomers. The results are interpreted on the basis of the X-ray diffraction analysis of 11 new compounds.

摘要

在互变异构体系IA⇌AC中,分别含有远程氨基/胺取代基的咪唑盐/N-杂环卡宾的M[N(SiMe₃)₂]金属片段的金属亲向性,通过其C亲碳性(R = tBu,M = Co,Fe)或NR亲氮性(R = Cy,M = Co,Fe;R = Mes,M = Fe)表现出来,并已根据空间和电子效应进行了合理化解释。[M{N(SiMe₃)₂}] / IA⇌AC体系的热解产物也取决于取代基,导致形成一种前所未有的重排氨基官能化aNHC Co络合物或开环金属酮亚胺;据推测它们源自不同的金属异构体。基于对11种新化合物的X射线衍射分析对结果进行了解释。

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