Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1306825 | Inorganica Chimica Acta | 2010 | 5 Pages |
Two dimeric head-on complexes of yttrium containing silico- and germanotungstate were isolated from the one-pot reaction of Y(NO3)3·6H2O with the lacunary Na10[MW9O34]·16H2O (M = Si and Ge) building blocks in an acetate buffer at pH 4.5. Both polyanions were structurally characterized using various solid-state analytics, such as single-crystal X-ray diffraction, single-crystal X-ray analysis shows that both polyanions crystallize in the monoclinic crystal system (S.G. P21/c). FT-IR spectroscopy, or thermogravimetric analysis. The stability of the polyanion in aqueous solution was studied by multinuclear NMR spectroscopy (183W, 89Y, 29Si, 13C, and 1H). As expected, the 183W NMR spectra display six peaks in the intensity ratio of 4:4:2:4:4:4 which indicates that both polyanions exist as dimeric entities in aqueous solution.
Graphical abstractYttrium containing head-on acetate complexes of silico- and germanotungstates are now accessible via a straightforward one-pot reaction. Multinuclear NMR investigations of these hybrid organic–inorganic polyoxometalates show that their dimeric solid-state structures are stable in aqueous solution.Figure optionsDownload full-size imageDownload as PowerPoint slide