...
首页> 外文期刊>Chemical science >Structural and mechanistic investigation of a cationic hydrogen-substituted ruthenium silylene catalyst for alkene hydrosllation
【24h】

Structural and mechanistic investigation of a cationic hydrogen-substituted ruthenium silylene catalyst for alkene hydrosllation

机译:阳离子氢取代的钌亚甲硅烷基烯烃裂解反应的结构和机理研究

获取原文
获取原文并翻译 | 示例
           

摘要

The cationic ruthenium silyiene complex [Cp~*(~iPr3P)Ru(H)2(SiHMes)][CB_(11)H6Br6], a catalyst for olefin hydrosilations with primary silanes, was isolated and characterized by X-ray crystallography. Relatively strong interactions between the silylene Si atom and Ru-H hydride ligands appear to reflect a highly electrophilic silicon center. The mechanism of olefin hydrosilation was examined by kinetics measurements and other experiments to provide the first experimentally determined mechanism for the catalytic cycle. This mechanism involves a fast, initial addition of the Si-H bond of the silylene complex to the olefin. Subsequent elimination of the product silane produces an unsaturated intermediate, which can be reversibly trapped by olefin or intercepted by the silane substrate. The latter reaction pathway involves activation of the reactant silane by Si-H oxidative addition and α-hydrogen migration to regenerate the key silylene intermediate.
机译:阳离子钌钌甲硅烷基络合物[Cp〜*(〜iPr3P)Ru(H)2(SiHMes)] [CB_(11)H6Br6]分离,并通过X射线晶体学对其进行了表征。甲硅烷基硅原子和Ru-H氢化物配体之间的相对较强的相互作用似乎反映出高度亲电子的硅中心。通过动力学测量和其他实验检查了烯烃氢化硅烷化的机理,以提供第一个实验确定的催化循环机理。该机理涉及将甲硅烷基络合物的Si-H键快速,初始地添加至烯烃。随后消除产物硅烷,产生不饱和中间体,该中间体可以可逆地被烯烃捕获或被硅烷底物拦截。后者的反应途径包括通过Si-H氧化加成反应活化反应硅烷,以及α-氢迁移以再生关键的甲硅烷基中间体。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号