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The role of basicity in selective C-H bond activation by transition metal-oxidos
被引:7
|作者:
Follmer, Alec H. H.
[1
]
Borovik, A. S.
[1
]
机构:
[1] Univ Calif Irvine, Dept Chem, Irvine, CA 92697 USA
关键词:
COUPLED ELECTRON-TRANSFER;
RAY-EMISSION SPECTROSCOPY;
HYDROGEN-ATOM TRANSFER;
NONHEME IRON(IV)-OXO COMPLEX;
OXO COMPLEXES;
IRON(IV)HYDROXIDE PK(A);
SPIN-STATE;
REACTIVITY;
LIGAND;
MECHANISMS;
D O I:
10.1039/d3dt01781h
中图分类号:
O61 [无机化学];
学科分类号:
070301 ;
081704 ;
摘要:
The development of (bio)catalysts capable of selectively activating strong C-H bonds is a continuing challenge in modern chemistry. In both metalloenzymes and synthetic systems capable of activating C-H bonds, transition metal-oxido intermediates serve as the active species for reactivity whose thermodynamic properties influence the bond strengths they are capable of activating. In this Frontier article, we present current ideas of how the basicity of transition metal-oxidos impacts their reactivity with C-H bonds and present new opportunities within this field. We highlight recent insights into the role basicity plays in the activation process and its influence on mechanism, as well as the important role that secondary coordination sphere effects, such as hydrogen bonds, in tuning the basicity of the metal-oxido species is discussed.
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页码:11005 / 11016
页数:12
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