Redox chemistry of the acetato-bridged clusters [M3(µ3-O)n(µ-O2CCH3)6(H2O)3]2+(M = Mo, W, n = 1, 2): reversible redox between mono-µ3-oxo d8MIII2MIVand d9MIII3forms

Abstract

A cyclic voltammogram of aqueous 0.1 mol dm(-3) triflic acid solutions of the d6 bioxo-capped M-M bonded cluster [Mo3(mu3-O)2(O2CCH3)6(H2O)3]2+ at a glassy carbon electrode at 25 degrees C gives rise to an irreversible 3e- cathodic wave to a d9 Mo(III)3 species at -0.8 V vs. SCE which on the return scan gives rise to two anodic waves at +0.05 V vs. SCE (E(1/2), 1e- reversible to d8 Mo(III)2Mo(IV)) and +0.48 V vs. SCE (2e- irreversible back to d6 Mo(IV)3). The number of electrons passed at each redox wave has been confirmed by redox titration and controlled potential electrolysis which resulted in 90% recovery of [Mo3(mu3-O)2(O2CCH3)6(H2O)3]2+ following electrochemical re-oxidation at +0.8 V. A corresponding CV study of the d8 monoxo-capped W(III)2W(IV) cluster [W3(mu3-O)(O2CCH3)6(H2O)3]2+ gives rise to a reversible 1e- cathodic process at -0.92 V vs. SCE to give the d9 W(III)3 species [W3(mu3-O)(O2CCH3)6(H2O)3]+; the first authentic example of a W(III) complex with coordinated water ligands. However the cluster is too unstable (O2/water sensitive) to allow isolation. Comparisons with the cv study on [Mo3(mu3-O)2(O2CCH3)6(H2O)3]2+ suggest irreversible reduction of this complex to monoxo-capped [Mo(III)3(mu3-O)(O2CCH3)6(H2O)3]+ followed by reversible oxidation to its d8 counterpart [Mo3(mu3-O)(O2CCH3)6(H2O)3]2+ (Mo(III)2Mo(IV)) and finally irreversible oxidation back to the starting bioxo-capped cluster. Exposing the d9 Mo(III)3 cluster to air (O2) however gives a different final product with evidence of break up of the acetate bridged framework. Corresponding redox processes on d6 [W3(mu3-O)2(O2CCH3)6(H2O)3]2+ are too cathodic to allow similar generation of the monoxo-capped W(III)3 and W(III)2W(IV) clusters at the electrode surface.