Progress in the preparation and characterization of silylene iron, cobalt and nickel complexes

被引:16
作者
Yang, Wenjing [1 ]
Dong, Yanhong [1 ]
Sun, Hongjian [1 ]
Li, Xiaoyan [1 ]
机构
[1] Shandong Univ, Minist Educ, Sch Chem & Chem Engn, Key Lab Special Funct Aggregated Mat, Shanda Nanlu 27, Jinan 250100, Peoples R China
关键词
N-HETEROCYCLIC SILYLENE; SILICON(II) COMPOUNDS; CATALYTIC-ACTIVITY; BOND ACTIVATION; REACTIVITY; LIGAND; COORDINATION; CLEAVAGE; DONOR; HYDROSILYLATION;
D O I
10.1039/d1dt00523e
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The synthesis and characterization of Fe, Co and Ni complexes supported by silylene ligands in the past ten years are summarized. Due to the decrease of the electron cloud density on the Si atom after coordination, the downfield shift of the Si-29 chemical shift is accompanied by the coordination between the free silylene ligand and metal. The strong electron-donating ability of silylene makes the metal center more electron-rich, which is conducive to the oxidative addition reaction in the metal center. In some cases, the coordination ability of silylene is stronger than those of phosphine and carbene ligands. Therefore, silylene transition metal complexes have better catalytic activity. The further challenges in this field are to develop new polydentate silylene ligands, synthesize chelate silylene-phosphine and silylene-carbene ligands, and design new silylene transition metal complexes for more catalytic research.
引用
收藏
页码:6766 / 6772
页数:7
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