摘要
The hydrothermal reactions of Keggin-type silicotungstate with rare-earth-transition-metal (RE-TM) heterometals in the presence of mixed ligands of oxalate and en (en = ethylenediamine) generate a novel two-dimensional (2D) organic-inorganic hybrid oxalate-bridging scandium-substituted silicotungstate. The complex [Cu(en)2(H2O)]2{[Cu(en)2(H2O)]2[Cu(en)2]2[(伪-SiW11O39)Sc(H2O)]2(C2O4)}路8H2O (1) has been further characterized by elemental analyses, powder X-ray diffraction (PXRD), IR spectra, thermogravimetric (TG) analyses, and single-crystal X-ray diffraction. X-ray structural analysis reveals that 1 exhibits the dimeric mono-Sc substituted Keggin [Sc(伪-SiW11O39)]210 鈭?/sup> subunits linked by the oxalate ligand, which further results in the 2D network architecture interconnected by [Cu(en)2]2 + coordination cations. Notably, 1 represents the first oxalate-bridging RE-TM heterometallic hybrid built by lacunary Keggin silicotungstate-supported RE derivatives and [Cu(en)2]2 + coordination cations. Furthermore, the TG curve of 1 displays two steps of slow weight loss in the range of 25-1000 掳C.