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Symmetry states of metalloporphyrin π-cation radicals, models for peroxidase compound I

Department of Chemistry, Virginia Commonwealth University, Richmond, VA 23284-2006, USA

Corresponding author, Department of Chemistry, Virginia Commonwealth University, Richmond, VA 23284-2006, USA.

Department of Environmental Sciences and Engineering, The University of North Carolina at Chapel Hill, NC 27599-7400, USA

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RAYMOND WEISS

Laboratoire de Cristallochimie et de Chimie Structurale (UMR 7513), Institut Le Bel, Université Louis Pasteur, 67070 Strasbourg, France

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DOMINIQUE MANDON

Laboratoire de Cristallochimie et de Chimie Structurale (UMR 7513), Institut Le Bel, Université Louis Pasteur, 67070 Strasbourg, France

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, and

ALFRED X. TRAUTWEIN

Institut für Physik, Medizinische Universität zu Lübeck, D-23538 Lübeck, Germany

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https://doi.org/10.1002/jpp.315Cited by:19 (Source: Crossref)

Abstract

Oxoferryl porphyrin π-cation radical active sites of compound I intermediates which are found in enzymes such as peroxidases and catalases have been extensively modeled by oxidized synthetic metalloporphyrins. The electronic symmetry states of these compounds were initially assigned on the basis of electronic absorption data. In recent years new experimental and theoretical results have become available which have led to a re-evaluation and modification of the original assignments. A historical perspective of these developments is provided in the context of recent NMR, resonance Raman, and other spectroscopic data and theoretical calculations for the synthetic models and enzymatic systems.

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