...
首页> 外文期刊>Chemistry: A European journal >Investigation of N-Heterocyclic Carbene-Supported Group 12 Triflates as Pre-catalysts for Hydrosilylation/Borylation
【24h】

Investigation of N-Heterocyclic Carbene-Supported Group 12 Triflates as Pre-catalysts for Hydrosilylation/Borylation

机译:N-杂环碳载第12族三氟甲磺酸酯作为氢化硅烷化/硼氢化反应的预催化剂的研究

获取原文
获取原文并翻译 | 示例

摘要

N-Heterocyclic carbene (NHC) complexes of Cd and Hg triflates (OTf) were prepared and their attempted conversion into rare cadmium and mercury hydrides was explored. In contrast to zinc, which forms stable [ZnH](+) complexes with NHCs, the heavier Cd and Hg congeners could not be formed; the increased instability of Cd-H and Hg-H units was rationalized with the aid of computations. It was also discovered that the dimeric adduct [IPr center dot Cd(mu-OTf)(2)](2) (IPr=[(HCNDipp)(2)C:]; Dipp= 2,6-iPr(2)C(6)H(3)) is an active precatalyst for the hydrosilylation and hydroborylation of hindered aldehydes and ketones. The related zinc congener was inactive as a catalyst highlighting a distinct advantage of using heavy Group 12 metals to promote catalytic hydrosilylation/borylation.
机译:制备了Cd和Hg三氟甲磺酸酯(OTf)的N-杂环卡宾(NHC)配合物,并尝试将其转化为稀有的镉和汞氢化物。与锌(与NHCs形成稳定的[ZnH](+)配合物)相反,锌不能形成较重的Cd和Hg同族元素; Cd-H和Hg-H单元增加的不稳定性通过计算得以合理化。还发现二聚加合物[IPr中心点Cd(mu-OTf)(2)](2)(IPr = [(HCNDipp)(2)C:]; Dipp = 2,6-iPr(2)C (6)H(3))是用于受阻醛和酮的氢化硅烷化和氢硼化的活性预催化剂。相关的锌同类物作为催化剂是无活性的,突出了使用重的12族金属来促进催化氢化硅烷化/硼化的显着优势。

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