The reaction of metal complexes with dioxygen (O-2) generally proceeds
in 1:1, 2:1, or 4:1 (metal:O-2) stoichiometry. A discrete, structural
ly characterized 3:1 product is presented. This mixed-valence trinucle
ar copper cluster, which contains copper in the highly oxidized trival
ent oxidation state, exhibits O-2 bond scission and intriguing structu
ral, spectroscopic, and redox properties. The relevance of this synthe
tic complex to the reduction of O-2 at the trinuclear active sites of
multicopper oxidases is discussed.