Abstract

Formal potentials of non-oxo vanadium complexes obtained by the cyclic voltammetry of solutions and of solid microcrystalline compounds are compared with potentiometrically determined stability constants of the corresponding oxovanadium(IV) complexes. The stability constants show a qualitative correlation with the formal potentials. The non-oxo complexes exhibit a reversible one-electron system VIV/VIII as well as VIV/VV in dichloromethane solution whereas the oxo complexes only show the transition between VIV and VV. Generally, the oxidation of non-oxo vanadium(IV) complexes proceeds at higher potentials than that of the corresponding oxovanadium(IV) species. The shift of the formal potentials is clearly correlated with the structure of the compounds.

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