首页> 美国卫生研究院文献>Acta Crystallographica Section E: Crystallographic Communications >Bistris­(ethyl­enediamine-κ2 NN′)cobalt(III) octa­kis-μ-3-oxido-hexa­deca-μ2-oxido-tetra­deca­oxido-μ12-tetra­oxo­silicato-octa­molybdenum(VI)hexa­vanadium(IVV) hexa­hydrate
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Bistris­(ethyl­enediamine-κ2 NN′)cobalt(III) octa­kis-μ-3-oxido-hexa­deca-μ2-oxido-tetra­deca­oxido-μ12-tetra­oxo­silicato-octa­molybdenum(VI)hexa­vanadium(IVV) hexa­hydrate

机译:Bis tris(乙二胺-κ2 NN)钴(III)八-μ-3-氧化十六碳-μ2-氧化十四碳-μ12-四氧硅基八钼(VI)六钒(IVV)六水合物

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摘要

The title compound, [Co(C2H8N2)3]2[SiMo8V4O40(VO)2]·6H2O, was prepared under hydro­thermal conditions. The asymmetric unit consists of a transition metal complex [Co(en)3]3+ cation (en is ethyl­enediamine), one half of an [SiMo8V4O40(VO)2]6− heteropolyanion, two solvent water mol­ecules in general positions and two half-mol­ecules of water located on a mirror plane. In the complex cation, the Co3+ ion is in a distorted octa­hedral coordination environment formed by six N atoms of the three chelating en ligands. One of the en ligands exhibits disorder of its aliphatic chain over two sets of sites of equal occupancy. The [SiMo8V4O40(VO)2]6− heteropolyanion is a four-electron reduced bivanadyl-capped α-Keggin-type molybdenum–vanadium–oxide cluster. In the crystal, it is located on a mirror plane, which results in disorder of the central tetra­hedral SiO4 group: the O atoms of this group occupy two sets of sites related by a mirror plane. Furthermore, all of the eight μ2-oxide groups are also disordered over two sets of sites with equal occupancy. There are extensive inter­molecular N—H⋯O hydrogen bonds between the complex cations and inorganic polyoxidoanions, leading to a three-dimensional supra­molecular network.
机译:在水热条件下制备标题化合物[Co(C2H8N2)3] 2 [SiMo8V4O40(VO)2]·6H2O。不对称单元由过渡金属络合物[Co(en)3] 3 + 阳离子(en为乙二胺),一半的[SiMo8V4O40(VO)2] 6-−组成。 sup>杂多阴离子,一般位置上有两个溶剂水分子,镜面上有两个半分子水。在复合阳离子中,Co 3 + 离子处于由三个螯合配体的六个N原子形成的扭曲的八面体配位环境中。一种en配体在两组相同占据的位点上显示出其脂族链的无序。 [SiMo8V 4 O 40 (VO) 2 ] 6-杂多阴离子是四电子还原的双钒基-封端的α-Keggin型钼-钒-氧化物簇。在晶体中,它位于镜平面上,导致中央四面体SiO 4 基团的无序:该组的O原子占据了与镜平面相关的两组位点。此外,所有八个μ 2 -氧化物基团在两组具有相同占有率的位点上也无序。复杂阳离子与无机多氧阴离子之间存在广泛的分子间N-H⋯O氢键,从而形成三维超分子网络。

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