卡宾
化学
硅氢加成
氢胺化
催化作用
位阻效应
沮丧的刘易斯对
过渡金属
广场互动
齿合度
组合化学
转移加氢
配体(生物化学)
胺化
有机化学
钌
金属
路易斯酸
受体
生物化学
作者
Abdollah Neshat,Piero Mastrorilli,Ali Mousavizadeh Mobarakeh
出处
期刊:Molecules
[MDPI AG]
日期:2021-12-24
卷期号:27 (1): 95-95
被引量:16
标识
DOI:10.3390/molecules27010095
摘要
Since the discovery of persistent carbenes by the isolation of 1,3-di-l-adamantylimidazol-2-ylidene by Arduengo and coworkers, we witnessed a fast growth in the design and applications of this class of ligands and their metal complexes. Modular synthesis and ease of electronic and steric adjustability made this class of sigma donors highly popular among chemists. While the nature of the metal-carbon bond in transition metal complexes bearing N-heterocyclic carbenes (NHCs) is predominantly considered to be neutral sigma or dative bonds, the strength of the bond is highly dependent on the energy match between the highest occupied molecular orbital (HOMO) of the NHC ligand and that of the metal ion. Because of their versatility, the coordination chemistry of NHC ligands with was explored with almost all transition metal ions. Other than the transition metals, NHCs are also capable of establishing a chemical bond with the main group elements. The advances in the catalytic applications of the NHC ligands linked with a second tether are discussed. For clarity, more frequently targeted catalytic reactions are considered first. Carbon-carbon coupling reactions, transfer hydrogenation of alkenes and carbonyl compounds, ketone hydrosilylation, and chiral catalysis are among highly popular reactions. Areas where the efficacy of the NHC based catalytic systems were explored to a lesser extent include CO2 reduction, C-H borylation, alkyl amination, and hydroamination reactions. Furthermore, the synthesis and applications of transition metal complexes are covered.
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