Anisotropic Polyoxometalate Cages Assembled via Layers of Heteroanion Templates
Q. Zheng, M. Kupper, W. Xuan, H. Oki, R. Tsunashima, D.-L. Long, L. Cronin
J. Am. Chem. Soc., 2019, 141, 13479–13486.
DOI : 10.1021/jacs.9b04533

Abstract: The synthesis of anisotropic redox-active polyoxometalates (POMs) that can switch between multiple states is critical for understanding the mechanism of assembly of structures with a high aspect ratio, as well as for their application in electronic devices. However, a synthetic methodology for the controlled growth of such clusters is lacking. Here we describe a strategy, using the heteroanion-directed assembly, to produce a family of 10 multi-layered, anisotropic POM cages templated by redox-active pyramidal heteroanions with the composition [W16Mo2O54(XO3)]n−, [W21Mo3O75/76(XO3)2]m−, and [W26Mo4O93(XO3)3]o− for the double, triple, and quadruple layered clusters, respectively. It was found that the introduction of reduced molybdate is essential for self-assembly and results in mixed-metal (W/Mo) and mixed-valence (WVI/MoV) POM cages, as confirmed by an array of analytical techniques. To probe the archetype in detail, a tetrabutyl ammonium (TBA) salt derivative of a fully oxidized two-layered cage is produced as a model structure to confirm that all the cages are a statistical mixture of isostructures with variable ratios of W/Mo. Finally, it was found that multilayered POM cages exhibit dipolar relaxations due to the presence of the mixed valence WVI/MoV metal centers, demonstrating their potential use for electronic materials..