Recent Advances on the Chemistry of Transition Metal Complexes with Monoanionic Bidentate Silyl Ligands

被引:6
作者
Batuecas, Maria [1 ]
Gomez-Espana, Alejandra [1 ,2 ]
Fernandez-Alvarez, Francisco J. [1 ]
机构
[1] Univ Zaragoza, Fac Ciencias, Dept Quim Inorgan, Inst Sintesis Quim & Catalisis Homogenea ISQCH,CSI, Plaza San Francisco, Zaragoza 50009, Spain
[2] Univ Pedag Nacl Francisco Morazan UPNFM, Ctr Invest & Innovac Educ CIIE, Tegucigalpa 11101, Honduras
来源
CHEMPLUSCHEM | 2024年 / 89卷 / 09期
关键词
silyl complexes; monoanionic bidentate silyl ligands; polydentate silyl ligands; transition metal complexes; SILICON BONDED COMPLEXES; ORGANOSILICON COMPOUNDS; MOLECULAR-STRUCTURE; COBALT COMPLEXES; C-H; CATALYTIC APPLICATION; IRON(II) COMPLEXES; SI-IR; CO2; REACTIVITY;
D O I
10.1002/cplu.202400162
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The chemistry of transition-metal (TM) complexes with monoanionic bidentate (kappa 2-L,Si) silyl ligands has considerably grown in recent years. This work summarizes the advances in the chemistry of TM-(kappa 2-L,Si) complexes (L=N-heterocycle, phosphine, N-heterocyclic carbene, thioether, ester, silylether or tetrylene). The most common synthetic method has been the oxidative addition of the Si-H bond to the metal center assisted by the coordination of L. The metal silicon bond distances in TM-(kappa 2-L,Si) complexes are in the range of metal-silyl bond distances. TM-(kappa 2-L,Si) complexes have proven to be effective catalysts for hydrosilylation and/or hydrogenation of unsaturated molecules among other processes. This work summarizes the advances in the chemistry of transition metal complexes with monoanionic bidentate ligands kappa 2-L,Si (L=N-heterocycle, phosphine, N-heterocyclic carbene, thioether, ester, silylether or tetrylene). image
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页数:22
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