Danopoulos Andreas A, Massard Alexandre, Frison Gilles, Braunstein Pierre
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.
Angew Chem Int Ed Engl. 2018 Oct 26;57(44):14550-14554. doi: 10.1002/anie.201808008. Epub 2018 Sep 19.
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.
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。