The crystal structures of hydro-thermally synthesized ( = 493 K, 7 d) thallium(I) digallium arsenic(V) hexa-kis-[hydrogenarsenate(V)], TlGaAs(HAsO), caes-ium digallium arsenic(V) hexa-kis-[hydrogenarsenate(V)], CsGaAs(HAsO), and caesium dialuminium arsenic(V) hexa-kis-[hydrogenarsenate(V)], CsAlAs(HAsO), were solved by single-crystal X-ray diffraction. The three compounds are isotypic and adopt the structure type of RbAlAs(HAsO) (), which itself represents a modification of the RbFe(HPO) structure type and consists of a tetra-hedral-octa-hedral framework in which the slightly disordered cations are located in channels. The three new compounds contain AsO octa-hedra assuming the topological role of O octa-hedra. The As-O bond lengths are among the shortest As-O bond lengths known so far in AsO octa-hedra.
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http://dx.doi.org/10.1107/S2056989018010721 | DOI Listing |
Acta Crystallogr E Crystallogr Commun
April 2024
TU Wien, Institute for Chemical Technologies and Analytics, Division of Structural Chemistry, Getreidemarkt 9/E164-05-1, 1060 Vienna, Austria.
The title compound, ammonium trinickel(II) hydrogen arsenate arsenate di-hydroxide, was synthesized under hydro-thermal conditions. Its crystal structure is isotypic with that of K[Cu(HAsO)(AsO)(OH)] and is characterized by pseudo-hexa-gonal (001) [NiAsO(OH)O(OH)] layers formed from vertex- and edge-sharing [NiO(OH)] octa-hedra and [AsO(OH)] tetra-hedra as the building units. The hydrogen atom of the OH group shows occupational disorder and was refined with a site occupation factor of 1/2, indicating the equal presence of [HAsO] and [AsO] groups.
View Article and Find Full Text PDFActa Crystallogr E Crystallogr Commun
February 2024
TU Wien, Institute for Chemical Technologies and Analytics, Division of Structural Chemistry, Getreidemarkt 9/E164-05-01, 1060 Vienna, Austria.
Single crystals of two basic cadmium phosphates, dicadmium orthophosphate hydroxide, Cd(PO)OH, and penta-cadmium bis-(orthophosphate) tetra-kis-(hydroxide), Cd(PO)(OH), were obtained under hydro-thermal conditions. Cd(PO)OH adopts the triplite [(Mn,Fe)(PO)F] structure type. Its asymmetric unit comprises two Cd, one P and five O sites, all situated at the general Wyckoff position 8 of space group 2/; two of the O atoms are positionally disordered over two sites, and the H atom could not be localized.
View Article and Find Full Text PDFActa Crystallogr E Crystallogr Commun
July 2022
Department of Chemistry, University of Aberdeen, Meston Walk, Aberdeen AB24 3UE, Scotland.
The isostructural compounds caesium deca-sodium tetra-zirconium nona-arsenate, CsNaZr(AsO), and caesium deca-sodium tetra-hafnium nona-arsenate, CsNaHf(AsO), arose as unexpected single-crystal products from the reactions of NaCO, MO ( = Zr, Hf) and AsO in a eutectic flux of NaCl and CsCl. They consist of O octa-hedra and AsO tetra-hedra sharing vertices to generate three-dimensional polyhedral networks encapsulating the caesium and sodium ions. The MO groups share all their vertices with adjacent As atoms but the As atoms have one or two 'terminal' O atoms not bonded to Zr or Hf.
View Article and Find Full Text PDFActa Crystallogr E Crystallogr Commun
September 2018
Naturhistorisches Museum Wien, Burgring 7, 1010 Wien, and Institut für Mineralogie und Kristallographie, Universität Wien, Althanstrasse 14, 1090 Wien, Austria.
The crystal structures of hydro-thermally synthesized ( = 493 K, 7-9 d) rubidium gallium bis-[hydrogenarsenate(V)], RbGa(HAsO), and rubidium digallium arsenic(V) hexa-[hydrogenarsenate(V)], RbGaAs(HAsO), were solved by single-crystal X-ray diffraction. Both compounds have tetra-hedral-octa-hedral framework topologies. The cations are located in channels of the respective framework.
View Article and Find Full Text PDFActa Crystallogr E Crystallogr Commun
August 2018
Naturhistorisches Museum, Burgring 7, 1010 Wien, Austria.
The crystal structures of hydro-thermally synthesized ( = 493 K, 7 d) thallium(I) digallium arsenic(V) hexa-kis-[hydrogenarsenate(V)], TlGaAs(HAsO), caes-ium digallium arsenic(V) hexa-kis-[hydrogenarsenate(V)], CsGaAs(HAsO), and caesium dialuminium arsenic(V) hexa-kis-[hydrogenarsenate(V)], CsAlAs(HAsO), were solved by single-crystal X-ray diffraction. The three compounds are isotypic and adopt the structure type of RbAlAs(HAsO) (), which itself represents a modification of the RbFe(HPO) structure type and consists of a tetra-hedral-octa-hedral framework in which the slightly disordered cations are located in channels. The three new compounds contain AsO octa-hedra assuming the topological role of O octa-hedra.
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