Hamza Hamadi, Zid Mohamed Faouzi, Driss Ahmed
Laboratoire de Matériaux et Cristallochimie, Faculté des Sciences de Tunis, Université de Tunis El Manar, 2092 Manar II Tunis, Tunisia.
Acta Crystallogr Sect E Struct Rep Online. 2010 Sep 4;66(Pt 10):i69. doi: 10.1107/S160053681003463X.
The title compound, sodium disilver arsenatotrimolybdate, Na(0.93 (1))Ag(2.07 (1))Mo(3)AsO(13), was prepared by a solid-state reaction. In the crystal structure, isolated AsO(4) tetra-hedra share corners with groups of three edge-sharing MoO(6) octa-hedra. This arrangement leads to the formation of anionic (1) (∞)Mo(3)AsO(13) ribbons extending parallel to [100]. The three metal sites show occupational disorder by Ag(I) and Na(I) cations, each with a different Ag:Na ratio. The metal cations are situated in the space between the ribbons and are surrounded by terminal O atoms of the ribbons in the form of distorted MO(7) polyhedra (M = Ag, Na) for distances < 3.0 Å. The title compound shows weak ionic conductivity. Structural relationships between different compounds in the quaternary systems M-Sb-P-O, M-Nb-P-O and M-Mo-As-O (M is Ag or an alkali metal) are also discussed.
标题化合物砷酸三钼二银钠(Na(0.93 (1))Ag(2.07 (1))Mo(3)AsO(13))通过固相反应制备。在晶体结构中,孤立的AsO(4)四面体与由三个共边的MoO(6)八面体组成的基团共用顶点。这种排列导致形成沿[100]方向延伸的阴离子(1) (∞)[Mo(3)AsO(13)]n 带。三个金属位点存在Ag(I)和Na(I)阳离子的占位无序,每个位点的Ag:Na比例不同。金属阳离子位于带之间的空间中,并以扭曲的MO(7)多面体(M = Ag、Na)形式被带的端基O原子包围,距离< 3.0 Å。标题化合物显示出弱离子导电性。还讨论了四元体系M-Sb-P-O、M-Nb-P-O和M-Mo-As-O(M为Ag或碱金属)中不同化合物之间的结构关系。