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Copper-Dioxygen and Copper-Oxo Species Relevant to Copper Oxygenases and Oxidases

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Metal-Oxo and Metal-Peroxo Species in Catalytic Oxidations

Part of the book series: Structure and Bonding ((STRUCTURE,volume 97))

Abstract

Copper proteins mediate both the transport and activation of dioxygen in a number of biological systems. The active sites of these proteins comprise mononuclear, dinuclear, and trinuclear copper centers, with the copper ions displaying a variety of coordination numbers and stereochemistries. Information regarding the mechanism by which these proteins activate dioxygen has been obtained by studies of the reactions of small molecule model copper complexes with dioxygen and its derivatives. Superoxo, peroxo, and bis(μ-oxo) intermediates in these reactions have recently been characterized by X-ray crystallography and this article concentrates on the structures of these intermediates, along with several Cu/ O2 complexes that have been well characterized by spectroscopic methods. The oxygenase-type reactivities of a number of copper complexes on reaction with dioxygen are also discussed.

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Authors and Affiliations

  1. Department of Chemistry, University of Otago, P.O. Box 56, Dunedin, New Zealand

    Allan G. Blackman

  2. Department of Chemistry and Center for Metals in Biocatalysis, University of Minnesota, 207 Pleasant St., SE, Minneapolis, MN, 55455, USA

    William B. Tolman

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  1. Allan G. Blackman
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  1. Laboratoire de Chimie de Coordination du CNRS, 205 route de Narbonne, 31077, Toulouse Cedex 4, France

    Bernard Meunier

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Blackman, A.G., Tolman, W.B. (2000). Copper-Dioxygen and Copper-Oxo Species Relevant to Copper Oxygenases and Oxidases. In: Meunier, B. (eds) Metal-Oxo and Metal-Peroxo Species in Catalytic Oxidations. Structure and Bonding, vol 97. Springer, Berlin, Heidelberg. https://doi.org/10.1007/3-540-46592-8_7

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