The electronic structure of the mixed-valence copper dimer [Cu₂{N(CH₂CH₂N[double bond, length half m-dash]CHCH[double bond, length half m-dash]NCH₂CH₂)₃N}]³⁺ ‡

Abstract

Fully delocalised mixed-valence (MV) copper dimers, {Cu^+1.5, Cu^+1.5}, have been identified both in proteins and in model complexes. An interpretation of the electronic transitions observed in the low-temperature magnetic circular dichroism and absorption spectra of one such dimer, [Cu₂L^imBT]³⁺, where L^imBT = N(CH₂CH₂N[double bond, length half m-dash] CHCH[double bond, length half m-dash]NCH₂CH₂)₃N, is presented. The spectrum is dominated by transitions within a set of energy levels derived from almost pure copper 3d orbitals of the [Cu₂]³⁺ core. Limited ligand covalency is found. The MV transition energy has been used to elucidate the valence delocalisation energy which is compared with the delocalisation energies in thiolate bridged MV copper dimers. The delocalisation energy of 7100 cm^–1 is almost entirely due to copper–copper σ overlap at a distance of 2.36 Å and represents a metal–metal bond (σ)²(σ *)¹ with bond order 0.5.

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