Quasireversible adducts of dioxygen with Cu(I) complexes are of interest as models for dioxygen transport proteins, for oxygen-dependent copper redox enzymes, and for low-molecular oxidation and oxygenation catalysts. Depending on ligand denticity and structural factors dioxygen binds in various geometries and metal:O2 ratios to the reduced copper centers. Kinetic investigations produce detailed mechanistic insight into the nature of coppers-dioxygen interaction. Heteronuclear FeO2Cu complexes with stabilities far beyond statistical expectation are obtained when 1:1 mixtures of suitable copper(I) complexes and appropriate Fe(II) porphyrins are treated with O2.
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