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The title compound H2SiW12O40·(CH3)2NH was synthesized in mixed solvent of aqueous and acetonitrile, and its crystal structure had been determined using single crystal X ray diffraction. The crystal belongs to monoclinic, space group C2/m, a=2.0654(4)nm, b=1.3306(3)nm, c=1.3194(3)nm, β=119.59(3)°, V=3.1531(11)nm3, Dc=3.606Mg·m-3, Z=2, R=0.0462, Rw=0.0836. The title compound comprises of a 2+ unit, a polyanion and a free (CH3)2NH molecule. The ESR spectrum of the title compound shows that charge transfer between organic groups and polyanion takes place under irradiation of the sunlight in solid state. The TG study of the title compound shows that it had four stages of the weight loss, and the increase of the decomposition temperature for the polyanion shows that the stability of the polyanion was enhanced due to the influence of Zn2+ ion. CCDC:175866.
The title compound H2SiW12O40 · (CH3) 2NH was synthesized in mixed solvent of aqueous and acetonitrile, and its crystal structure had been determined using single crystal X-ray diffraction. The crystal belongs to monoclinic, space group C2 / m, a = 2.0654 ) nm, b = 1.3306 (3) nm, c = 1.3194 (3) nm, β = 119.59 (3) °, V = 3.1531 (11) nm3, Dc = 3.606 Mg · m-3, 0.0462, Rw = 0.0836. The title compound comprises a 2+ unit, a polyanion and a free (CH3) 2NH molecule. The ESR spectrum of the title compound shows that charge transfer between organic groups and polyanion takes place under irradiation of the sunlight in solid state. The TG study of the title compound that that had had four stages of the weight loss, and the increase of the decomposition temperature for the polyanion was that the stability of the polyanion was enhanced due to the influence of Zn2 + ion. CCDC : 175866.