C-H Bond Activation and Organometallic Intermediates on Isolated Metal Centers on Oxide Surfaces

被引:386
作者
Coperet, Christophe [1 ]
机构
[1] Univ Lyon 1, Inst Chim Lyon, C2P2, UMR 5265,CNRS CPE,CPE Lyon F308, F-69616 Villeurbanne, France
关键词
DENSITY-FUNCTIONAL THEORY; OLEFIN METATHESIS CATALYSTS; SUPPORTED TANTALUM HYDRIDE; SOLID-STATE NMR; HIGHLY REACTIVE ORGANOLANTHANIDES; METHANE PARTIAL OXIDATION; DIFFUSE-REFLECTANCE SPECTROSCOPY; LOW-TEMPERATURE HYDROGENOLYSIS; BUTANE SELECTIVE OXIDATION; GALLIUM-LOADED CATALYSTS;
D O I
10.1021/cr900122p
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A study was conducted to investigate C-H bond activation and organometallic intermediates on isolated metal centers on oxide surfaces. It was demonstrated that C-H bond activation was a ubiquitous process in heterogeneous catalysis that involved various types of mechanisms and intermediates. The study focused on investigating processes that involved C-H bond activation of alkenes and aromatics on isolated metal centers of surface oxide materials leading to organometallic species and intermediates. One potential pathway in alkene dehydrogenation involved the formation of a metal-alkyl intermediate that underwent β-H elimination and generated an alkene. It was demonstrated that cofeeding CO2 increased the activity and the stability of these nonoxidative dehydrogenation catalysts, as CO2 played the role of a mild oxidant and prevented coke formation.
引用
收藏
页码:656 / 680
页数:25
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