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Electrochemical Behaviour of merdional tris(2-pyridinethiolato)Cobalt(Ⅲ) in Dimethylformamide Solution

  • Published : 1997.05.20

Abstract

Electrochemical behavior of mer-tris(2-pyridinethiolato)cobalt(Ⅲ) in dimethylformamide was studied on a platinum electrode by means of cyclic voltammetry, chronoamperometry, and chronocoulometry. It was found that the neutral complex molecule was electroactive between the potential region of 1.0 and - 1.2 V vs. a nonaqueous Ag/Ag+ electrode. The Co(Ⅲ) complex was reversibly reduced to Co(Ⅱ) species by one-electron transfer at about - 1.1 V, followed by an irreversible dissociation reaction. However, the oxidation process at around 0.8 V, was responsible for an irreversible two-electron transfer that occurred at a ligand site.

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References

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