Citation: CHEN Wu-Hua, ZHANG Zhu-Sen, HU Zhi-Biao, MI Jin-Xiao. The First Hybrid Wells-Dawson-type Polytungstate Monosupported by Cd-coordination Complex via Di-bridging O-atom[J]. Chinese Journal of Structural Chemistry, ;2014, 33(10): 1550-1559.
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Polyoxometalates (POMs) with Cd-coordination complexes acting as supporting units are rarely reported. The linkage of the supporting units with inorganic building block (polyanion) is generally established on terminal O-atoms, but scarcely via bridging O-atoms. By introducing liquid small organic molecule (pyridine, C5NH5) as assistant "structure-directing agent", we obtained a novel organic-inorganic hybrid polytungstate, (Hpy)4[Cd(phen)2(P2W18O62)]·nH2O (1, n≈3, py=pyridine, phen=1,10-phenanthroline), under hydrothermal conditions. The single-crystal X-ray diffraction analysis shows that 1 is the first compound containing an asymmetric heteropolyanion,[Cd(phen)2(P2W18O62)]4-, a Wells-Dawson-type polyanion monosupported by Cd-coordination complex via di-bridging O-atoms.
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