Participation of Electron Transfer Process in Rate-Limiting Step of Aromatic Hydroxylation Reactions by Compound I Models of Heme Enzymes

被引:63
作者
Asaka, Maaya [1 ]
Fujii, Hiroshi [1 ]
机构
[1] Nara Womens Univ, Grad Sch Humanities & Sci, Dept Chem, Nara 6308506, Japan
关键词
ACCURATE OXIDATION POTENTIALS; CATION RADICAL COMPLEXES; CYTOCHROME-P450; ENZYMES; BIPHENYL DERIVATIVES; MECHANISM; PORPHYRIN; BENZENE; METABOLISM; KINETICS; PHENOLS;
D O I
10.1021/jacs.6b03223
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Hydroxylation reactions of aromatic rings are key reactions in various biological and chemical processes. In spite of their significance, no consensus mechanism has been established. Here we performed Marcus plot analysis for aromatic hydroxylation reactions with oxoiron(IV) porphyrin pi-cation radical complexes (compound I). Although many recent studies support the mechanism involving direct electrophilic attack of compound I, the slopes of the Marcus plots indicate a significant contribution of an electron transfer process in the rate-limiting step, leading us to propose a new reaction mechanism in which the electron transfer process between an aromatic compound and compound I is in equilibrium in a solvent cage and coupled with the subsequent bond formation process.
引用
收藏
页码:8048 / 8051
页数:4
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