High stable sandwich-type polyoxometallates based on . Synthesis, chemical properties and characterization of [(A-β-SiW9O34)2(MOH2)3CO3] (M = Y and Yb)

Highly hydrolytic and thermally stable sandwich-type polyoxometallates of (A-β-SiW₉O₃₄)₂(MOH₂)₃CO₃]¹³⁻ (M = Y³⁺ and Yb³⁺) have been synthesized at room temperature by stoichiometric reactions of the trilacunary ligand with M³⁺ in 0.1 M carbonate solution. The new complexes were isolated as sodium and mixed sodium/potassium salts and were characterized by elemental analysis, IR, ¹³C and ²⁹Si NMR, UV–Vis spectroscopy, TGA, DSC and single crystal structure analysis. The crystal structure of the complexes consist of two lacunary Keggin moieties which are linked by a (H₂OMO)₃C belt into an assembly of virtual C₂ symmetry. Each M³⁺ ion adopts a mono-capped trigonal-prismatic coordination. The C₂ axis of the complexes and the local 3-fold axis of the MO₆ group lies in the (H₂OMO)₃C belt plane. The trigonal prismatic geometry is achieved by the two terminal oxygen atoms of an edge shared pair of WO₆ octahedra from each moiety and two oxygen from the belt, and the cap by one external water ligand. The hydrolytic and thermal stabilities of the complexes and the reasons that prove the retention of the isomeric form of the trilacunary ligand upon complexation are discussed.