Abstract
By incorporating phosphorus(III)-based anions into a polyoxometalate cage, a new type of tungsten-based unconventional Dawson-like cluster, [W18O56(HPIIIO3)2(H2O)2]8-, was isolated, in which the reaction of the two phosphite anions [HPO3]2- within the {W18O56} cage could be followed spectroscopically. As well as full X-ray crystallographic analysis, we studied the reactivity of the cluster using both solution-state NMR spectroscopy and mass spectrometry. These techniques show that the cluster undergoes a structural rearrangement in solution whereby the {HPO3} moieties dimerize to form a weakly interacting (O3PH···HPO3) moiety. In the crystalline state the cluster exhibits a thermally triggered oxidation of the two PIII template moieties to form PVcenters (phosphite to phosphate), commensurate with the transformation of the cage into a Wells-Dawson {W18O54} cluster.
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Zheng, Q., Vilà-Nadal, L., Busche, C., Mathieson, J. S., Long, D. L., & Cronin, L. (2015). Following the Reaction of Heteroanions inside a {W18O56} Polyoxometalate Nanocage by NMR Spectroscopy and Mass Spectrometry. Angewandte Chemie - International Edition, 54(27), 7895–7899. https://doi.org/10.1002/anie.201502295
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