issue contents
June 1996 issue
inorganic compounds
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The composition of Sr(ReO4)2.2H2O has been reconfirmed as the dihydrate. The structure contains trigonal bipyramidal disordered ReO4 groups with two partially occupied
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CeCu1-xBi2 is isotypic with ZrCuSi2, and has a layered structure composed of two-dimensional Bi layers formed from closely arranged Bi atoms in a square-lattice array and CeBiCu slabs formed from edge-sharing distorted CeBiCu4 octahedra.
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Mg2As2O7.2H2O and Zn2As2O7.2H2O have been prepared by hydrothermal methods. They are isotypic and have a framework structure characterized by zigzag infinite chains of edge-sharing MO6 octahedra linked by As2O7 groups to form a three-dimensional structure containing intersecting tunnels.
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In Bi7.5Y0.5O12 and Bi7.68Ti0.32O12.16, Y and Ti atoms replace Bi atoms in the β-Bi2O3 structure and additional O atoms are incorporated. This causes local disorder and irregular displacements of all the atoms.
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The structure of PdTe2 has been redetermined. The structure is two-dimensional and comprises layers of edge-sharing PdTe6 octahedra.
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The crystal structure of Si2I6, prepared by heating SiI4 with metallic silver, is reported. The Si2I6 molecules have a staggered conformation.
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Potassium molybdyl arsenate is built up from MoO6 octahedra and As2O7 groups sharing corners to form layers. The two O atoms of the molybdyl group remain unshared and show short Mo-O distances. The K+ ions are located in the interlayer space.
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The β-Ga2O3 structure is formed from a distorted cubic close packing of O atoms with Ga in both octahedral and tetrahedral sites, and contains double chains of edge-sharing octahedra connected by corner-sharing tetrahedra.
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The structure of Ba3[V10O28].19H2O is built up from decavanadate ions linked by hydrated Ba2+ cations. There are two crystallographically independent decavanadate ions in the asymmetric unit.
metal-organic compounds
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organic compounds
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addenda and errata
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Addenda to Acta Cryst. (1992), C 48, 655-657 and Acta Cryst. (1993), C 49, 684-687.