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首页> 外文期刊>Zeitschrift fur Anorganische und Allgemeine Chemie >The first vanadium(III) borophosphate: Synthesis and crystal structure of CsV3(H2O)(2)[B2P3O16(OH)(4)] [German]
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The first vanadium(III) borophosphate: Synthesis and crystal structure of CsV3(H2O)(2)[B2P3O16(OH)(4)] [German]

机译:第一钒硼化钒(III):CsV3(H2O)(2)[B2P3O16(OH)(4)]的合成和晶体结构[德语]

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CsV3(H2O)(2)[B2P4O16(OH)(4)] was prepared under mild hydrothermal conditions (T = 165 degrees C) from mixtures of CsOH(aq), VCl3, H3BO3, and H3PO4 (molar ratio 1:1.1.2). The crystal structure was determined by X-ray single crystal methods (monoclinic; space group C2/m, No. 12). a = 958.82(15) pm, b = 1840.8(4) pm, c = 503.49(3) pm; beta = 110.675(4)degrees; Z = 2. The anionic partial structure contains oligomeric units [BP2O8(OH)(2)](5-), which are built up by a central BO2(OH)(2) tetrahedron and two PO4 tetrahedra sharing common corners. V-III is octahedrally coordinated by oxygen of adjacent phosphate tetrahedra and OH groups of berate tetrahedra as well as oxygen of phosphate tetrahedra and H2O molecules, respectively (coordination octahedra VO4(OH)(2) and VO4(H2O)(2)) The oxidation state +3 for vanadium was confirmed by measurements of the magnetic susceptibility. The trimeric borophosphate groups are connected via vanadium centres to form layers with octahedra-tetrahedra ring systems, which are likewise linked via V-III coordination octahedra. Overall, a tkree-dimensional framework constructed from VO4(OH)(2) and VO4(H2O)(2) octahedra as well as BO2(OH)(2) and PO4 tetrahedra results. The structure contains channels running along [001], which are occupied by Cs+ in a distorted octahedral coordination (CsO4(H2O)(2)). [References: 28]
机译:CsV3(H2O)(2)[B2P4O16(OH)(4)]是在温和的水热条件下(T = 165摄氏度)由CsOH(aq),VCl3,H3BO3和H3PO4(摩尔比为1:1.1)的混合物制备的。 2)。通过X射线单晶方法(单斜晶; C2 / m空间群,第12号)确定晶体结构。 a = 958.82(15)pm,b = 1840.8(4)pm,c = 503.49(3)pm; beta = 110.675(4)度; Z =2。阴离子部分结构包含低聚单元[BP2O8(OH)(2)](5-),它们由一个中央BO2(OH)(2)四面体和两个共享共同角的PO4四面体组成。 V-III的八面体分别与相邻的磷酸酯四面体的氧和贝酸酯四面体的OH基团以及磷酸四面体和H2O分子的氧八面体配位(配位八面体VO4(OH)(2)和VO4(H2O)(2))。通过测量磁化率证实钒的氧化态为+3。三聚硼磷酸盐基团通过钒中心连接,形成具有八面体-四面体环系统的层,八面体-四面体环系统同样通过V-III配位八面体连接。总的来说,得到了由VO4(OH)(2)和VO4(H2O)(2)八面体以及BO2(OH)(2)和PO4四面体构成的三维结构。该结构包含沿[001]延伸的通道,这些通道在变形的八面体坐标(CsO4(H2O)(2))中被Cs +占据。 [参考:28]

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