Synthesis of π-conjugated cobaltadithiolene cyclotrimers and significant effects of electrolyte cation and solvent on their electrochemical, optical and magnetic properties †

Abstract

A new class of cobalt cyclic trinuclear complexes with four fused aromatic rings, [Co₃(η-C₅H₅)₃(S₆C₆)] and [Co₃(η-C₅H₄Me)₃(S₆C₆)], was synthesized by a condensation reaction of [Co(η-C₅H₅)(S₂C₂H₂)] and [Co(η-C₅H₄Me)(S₂C₂H₂)], respectively, in aqueous halogenoacid solution. The complexes undergo reversible three-step 1e^– reductions in aprotic media forming two mixed-valence states, with overall charges 1– and 2–. The thermodynamic stability of the mixed-valence complexes estimated from the redox potential differences and the degree of internuclear electronic interaction evaluated from the intervalence-transfer bands depends markedly on the size of the electrolyte cation and the solvent polarity; larger cations and more polar solvents increase the stability and the electronic interaction. The EPR spectra of [Co₃(η-C₅H₅)₃(S₆C₆)] reduced by [Co(η-C₅Me₅)₂] in propylene carbonate (pc) indicate that the 1– and 3– species are paramagnetic with S = ½, whereas the 3– species formed by reduction with Na in thf gives a spectrum of the quartet state (S = [/]) denoting ferromagnetic interaction. This difference is attributed to a weaker internuclear interaction caused by a stronger electrostatic effect of the smaller counter ion, Na⁺ in thf, compared to [Co(η-C₅Me₅)₂]⁺ in pc.

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