Design Strategy of Metal Nanoparticle Catalysis for C-H Bond Activation Reactions

被引:1
|
作者
Hasegawa, Shingo [1 ]
Motokura, Ken [1 ]
机构
[1] Yokohama Natl Univ, Dept Chem & Life Sci, 79-5 Tokiwadai,Hodogaya Ku, Yokohama 2408501, Japan
关键词
Metal nanoparticle; C-H bond activation; Reverse hydrogen spillover; Ligand modification; Bimetallic nanoparticle; AEROBIC DEHYDROGENATION; HYDROGEN SPILLOVER; COUPLING REACTIONS; PALLADIUM; PD; OXIDATION; ENONES; RH;
D O I
10.1002/cctc.202301531
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
C-H bond activation reactions facilitate highly efficient molecular transformations without requiring pre-activating substrates. While the majority of reported reaction systems for C-H activation rely on metal complexes, certain reactions have demonstrated unique or superior catalysis of metal nanoparticles. This Concept article seeks to delineate recent reports that examine the novel catalysis and design strategy of supported metal nanoparticles for C-H bond activation reactions. These reactions include oxidative homocoupling of arenes, dehydrogenative alkylation of benzenes, selective H/D exchange reactions, and alpha,beta-dehydrogenation of ketones. Supported metal nanoparticles have attracted growing research interest as promising sustainable catalysts. This Concept article will describe recent studies that explored the novel catalytic functions and designing methods of metal nanoparticles for C-H bond activation reactions. Examples include oxidative homocoupling of arenes, dehydrogenative alkylation of benzenes, selective H/D exchange reactions, and alpha,beta-dehydrogenation of ketones. image
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页数:6
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