Electronic structure and reactivity of high-valent oxo iron porphyrins

被引:211
作者
Fujii, H [1 ]
机构
[1] Okazaki Natl Res Inst, Inst Mol Sci, Okazaki, Aichi 4448585, Japan
[2] Okazaki Natl Res Inst, Ctr Integrat Biosci, Okazaki, Aichi 4448585, Japan
关键词
cytochrome P450; peroxidase; catalase; heme; porphyrin;
D O I
10.1016/S0010-8545(01)00441-6
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
High valent oxo iron porphyrins have been prepared and characterized as models for compounds-I and compounds-II in heme enzymes. In this review, we survey studies of high valent oxo iron porphyrin complexes. Spectroscopic properties and reactivities of oxo iron(IV) porphyrin pi-cation radical complexes are summarized. Electron-withdrawing effects of meso-substituents and pyrrole beta-substituents on the electronic structure of oxo iron(IV) porphyrin pi-cation radicals are discussed. The effect of the axial ligand is also reviewed. Isoelectronic forms of oxo iron(IV) porphyrin pi-cation radical are reviewed. We have summarized the synthesis and characterization of oxo iron(IV) porphyrins as models for compounds-II. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:51 / 60
页数:10
相关论文
共 49 条
[1]   OXIDATION OF RED FERRYL [(FEIVO)2+]PORPHYRIN COMPLEXES TO GREEN FERRYL [(FEIVO)2+]PORPHYRIN RADICAL COMPLEXES [J].
BALCH, AL ;
LATOSGRAZYNSKI, L ;
RENNER, MW .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1985, 107 (10) :2983-2985
[2]  
BALCH AL, 1984, J AM CHEM SOC, V106, P7779, DOI 10.1021/ja00337a022
[3]   EPR AND ENDOR DETECTION OF COMPOUND-I FROM MICROCOCCUS-LYSODEIKTICUS CATALASE [J].
BENECKY, MJ ;
FREW, JE ;
SCOWEN, N ;
JONES, P ;
HOFFMAN, BM .
BIOCHEMISTRY, 1993, 32 (44) :11929-11933
[4]   MOSSBAUER-EFFECT STUDY OF TIGHT SPIN COUPLING IN OXIDIZED CHLORO-5,10,15,20-TETRA(MESITYL)PORPHYRINATOIRON(III) [J].
BOSO, B ;
LANG, G ;
MCMURRY, TJ ;
GROVES, JT .
JOURNAL OF CHEMICAL PHYSICS, 1983, 79 (03) :1122-1126
[5]   ROLE OF FERRYL (FEO2+) COMPLEXES IN OXYGEN ATOM TRANSFER-REACTIONS - MECHANISM OF IRON(II) PORPHYRIN CATALYZED OXYGENATION OF TRIPHENYLPHOSPHINE [J].
CHIN, DH ;
LAMAR, GN ;
BALCH, AL .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1980, 102 (18) :5945-5947
[6]   FORMATION OF PORPHYRIN FERRYL (FEO2+) COMPLEXES THROUGH THE ADDITION OF NITROGEN BASES TO PEROXO-BRIDGED IRON(III) PORPHYRINS [J].
CHIN, DH ;
BALCH, AL ;
LAMAR, GN .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1980, 102 (04) :1446-1448
[7]   Insensitivity of vanadyl-oxygen bond strengths to radical type (2A1u vs 2A2u) in vanadyl porphyrin cation radicals [J].
Czarnecki, K ;
Proniewicz, LM ;
Fujii, H ;
Ji, D ;
Czernuszewicz, RS ;
Kincaid, JR .
INORGANIC CHEMISTRY, 1999, 38 (07) :1543-1547
[8]   Resonance Raman spectrum of a (2)A(1u) ferryl porphyrin pi-cation radical [J].
Czarnecki, K ;
Proniewicz, LM ;
Fujii, H ;
Kincaid, JR .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1996, 118 (19) :4680-4685
[9]   Direct resonance Raman evidence for a trans influence on the ferryl fragment in models of compound I intermediates of heme enzymes [J].
Czarnecki, K ;
Nimri, S ;
Gross, Z ;
Proniewicz, LM ;
Kincaid, JR .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1996, 118 (12) :2929-2935
[10]   Resonance raman spectra of legitimate models for the ubiquitous compound I intermediates of oxidative heme enzymes [J].
Czarnecki, K ;
Kincaid, JR ;
Fujii, H .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1999, 121 (34) :7953-7954