Azpeitia S, Martínez-Martínez A J, Garralda M A, Weller A S, Huertos M A
Department of Applied Chemistry, University of Basque Country (UPV/EHU), 20080 San Sebastián, Spain.
Dalton Trans. 2020 May 7;49(17):5416-5419. doi: 10.1039/d0dt00725k. Epub 2020 Apr 6.
An easy, direct and room temperature silicon-carbon bond activation is reported. The reaction of [RhCl(coe)] with the silane Si(Me)(o-CHSMe) in the presence of an halide extractor provokes a Si-CH bond cleavage yielding a cationic silyl-methyl-Rh(iii). In contrast, if the reaction is performed using the Rh(i) bis-alkene dimers, [RhCl(cod)] or [RhCl(nbd)], the Si-CH bond activation does not occur.
报道了一种简单、直接且在室温下的硅-碳键活化反应。在卤化物萃取剂存在下,[RhCl(coe)]与硅烷Si(Me)(o-CHSMe)反应会引发Si-CH键断裂,生成阳离子型甲硅烷基-甲基-Rh(iii)。相比之下,如果使用Rh(i)双烯烃二聚体[RhCl(cod)]或[RhCl(nbd)]进行该反应,则不会发生Si-CH键活化。