Leveraging a reduced polyoxomolybdate-alkoxide cluster for the formation of a stable U(v) sandwich complex

Abstract

The synthesis and characterization of a series of (TBA)₂[M{Mo₅O₁₃(OMe)₄NO}₂] (M = Zr, Hf, Th, and U) sandwich complexes is reported. A preformed lacunary, Lindqvist-type, polyoxomolybdate-alkoxide cluster provides access to first examples of actinide-polyoxomolybdate sandwich complexes isolated under non-aqueous conditions. Incorporation of metal(IV) cations into this framework was found to “switch on” reversible redox chemistry at the {Mo₅} ligands, with the Zr and Hf containing complexes accepting up to two electrons, while the Th and U derivates accommodate as many as four additional electrons. The enhancement of the redox properties of the cluster upon actinide incorporation is an exciting observation, presenting actinide “doping” as a novel approach for accessing functional redox-active materials. Oxidation of the uranium containing sandwich complex (TBA)₂[U{Mo₅O₁₃(OMe)₄NO}₂], chemically or electrochemically, allows access to the U(V) centered species, which was characterized both spectroscopically and by single crystal X-ray diffraction. This represents the first example of a U(V)-polyoxometalate sandwich complex to be isolated and structurally characterized.