Abstract
Two tris-functionalized Zr4IV-substituted germanetungstates H9KNa2[Zr4(μ3-O)2(tris)2(α-GeW10O37)2]·26H2O (1) and H2K6Na4[Zr4(μ3-O)2(tris)2(α-GeW10O37)2]·20H2O (2) (tris = tris(hydroxymethyl)aminomethane) have been made under mild hydrothermal conditions and characterized by elemental analysis, IR spectra, diffuse reflectance spectra, thermogravimetric analysis, single-crystal X-ray diffraction and powder X-ray diffraction, respectively. 1–2 possess similar sandwich-type polyoxoanion structure built by a tetra-ZrIV cluster and two divacant [α-GeW10O37]10 − building blocks. 1 and 2 represent the first [Zr4(μ3-O)2(tris)2]10+-substituted germanotungstates functionalized by tris ligands with O– and N-donors.
Original language | English |
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Pages (from-to) | 32-36 |
Number of pages | 5 |
Journal | Inorganic Chemistry Communications |
Volume | 85 |
DOIs | |
Publication status | Published - Nov 2017 |
Keywords
- Hydrothermal synthesis
- Polyoxometalate
- Tris-functionalized
- Zirconium(IV)-substituted cluster