Holthausen Michael H, Mallov Ian, Stephan Douglas W
Department of Chemistry, 80 St George St University of Toronto, Toronto, Ontario, M5S3H6 Canada.
Dalton Trans. 2014 Oct 28;43(40):15201-11. doi: 10.1039/c4dt02406k. Epub 2014 Sep 3.
The phosphinimines R3PNSiMe3 (R = t-Bu: 1a, R = Cy: 1b, R = Et: 1c, R = Ph: 1d) are reacted with a series of chloro and fluoroboranes (9Cl-9-BBN, (C6F5)2BCl, PhBCl2 and Mes2BF) to access a family of phosphinimine-substituted boranes (2a-d, 3b-d, 4c,d and 6a,b) via Me3SiX elimination (X = Cl, F). The steric and electronic factors governing the formation of monomeric or dimeric products (7c,d) are presented. In addition, in some cases a Lewis acid mediated exchange of Si-bonded methyl groups for a chloro-substituent was observed (5a,b). Based on the phosphinimine-substituted boranes, a series of borenium ion salts (8b-d, 9c, 10b-d) was prepared upon reaction with MeOTf. All compounds were fully characterized and a number of molecular structures were determined by X-ray diffraction.
膦亚胺R3PNSiMe3(R = t-Bu:1a,R = Cy:1b,R = Et:1c,R = Ph:1d)与一系列氯代硼烷和氟硼烷(9Cl-9-BBN、(C6F5)2BCl、PhBCl2和Mes2BF)反应,通过消除Me3SiX(X = Cl、F)得到一系列膦亚胺取代的硼烷(2a-d、3b-d、4c,d和6a,b)。阐述了控制单体或二聚体产物(7c,d)形成的空间和电子因素。此外,在某些情况下,观察到路易斯酸介导的与硅键合的甲基被氯取代基交换的现象(5a,b)。基于膦亚胺取代的硼烷,与MeOTf反应制备了一系列硼正离子盐(8b-d、9c、10b-d)。所有化合物均得到充分表征,并且通过X射线衍射确定了一些分子结构。