Hydrothermal Crystal Growth and Structure Determination of Double Hydroxides LiSb(OH)6, BaSn(OH)6, and SrSn(OH)6
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文摘
Colorless single crystals of LiSb(OH)6, SrSn(OH)6, and BaSn(OH)6, which are useful as precursors for the synthesis of LiSbO3, SrSnO3, and BaSnO3, were synthesized by a low-temperature hydrothermal method using a Teflon-lined autoclave at 380 K. The crystal structures were determined by single-crystal X-ray diffraction measurements. LiSb(OH)6 crystallizes in the trigonal space group P3虆1m with a = 5.3812(3)A, c = 9.8195(7)A, V = 246.25(3)A3, Z = 2. In this layered structure, [Li2Sb(OH)6]+ and [Sb(OH)6]鈭?/sup> layers are alternately stacked along the c-direction. The [Li2Sb(OH)6]+ layer can be regarded as a cation-ordered CdCl2 layer. The [Sb(OH)6)]鈭?/sup> layer is built up from isolated [Sb(OH)6]鈭?/sup> octahedra, which are linked to each other via hydrogen bonding within the layer. BaSn(OH)6 and SrSn(OH)6 crystallize with monoclinic P21/n space group symmetry. The monoclinic structure possesses a CsCl-type packing of Ba2+/Sr2+ cations and [Sn(OH)6]2鈥?/sup> anions. The [Sn(OH)6]2鈥?/sup> polyhedra are connected to each other through hydrogen bonding to form a three-dimensional framework. The factors that favor these hitherto unknown crystal structures are discussed using a structure map that compares various M(OH)3 and M鈥睲鈥?OH)6 compounds.

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