Active sites and mechanisms of bioinspired oxidation with H2O2, catalyzed by non-heme Fe and related Mn complexes

被引:200
作者
Bryliakov, Konstantin P. [1 ,2 ]
Talsi, Evgenii P. [1 ,2 ]
机构
[1] Boreskov Inst Catalysis, Novosibirsk 630090, Russia
[2] Novosibirsk State Univ, Novosibirsk 630090, Russia
基金
俄罗斯科学基金会;
关键词
Active site; Bioinspired; Iron; Manganese; Oxidation; Mechanism; HIGH-VALENT IRON; KETOGLUTARATE DIOXYGENASE TAUD; OLEFIN CIS-DIHYDROXYLATION; O-O BOND; 2-HIS-1-CARBOXYLATE FACIAL TRIAD; ELECTRON-DEFICIENT OLEFINS; SPIN OXOIRON(IV) COMPLEX; OXYGEN-EVOLVING COMPLEX; C-H ACTIVATION; MANGANESE 1,4,7-TRIMETHYL-1,4,7-TRIAZACYCLONONANE COMPLEXES;
D O I
10.1016/j.ccr.2014.06.009
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
In the last two decades, considerable efforts were invested in the search for synthetic iron and manganese catalysts with nonporphyrinic ligands, mimicking metalloenzymes in the oxygenation at C-H and C=C bonds of organic molecules. In many cases, the detailed knowledge of intimate reaction mechanisms and of the nature of active sites was critical for the rational design of biomimetic catalysts with predictable reactivities. This review discusses the up-to-date mechanistic landscape of non-heme iron and manganese catalyzed oxidations of olefinic groups and aliphatic C-H groups with H2O2. (C) 2014 Published by Elsevier B.V.
引用
收藏
页码:73 / 96
页数:24
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