Flux syntheses and single-crystal structures of CsNa10M4(AsO4)9 (M = Zr, Hf)

被引:0
作者
Harrison, William T. A. [1 ]
机构
[1] Univ Aberdeen, Dept Chem, Meston Walk, Aberdeen AB24 3UE, Scotland
来源
ACTA CRYSTALLOGRAPHICA SECTION E-CRYSTALLOGRAPHIC COMMUNICATIONS | 2022年 / 78卷
关键词
crystal structure; zirconium; hafnium; arsenate; ionic conduction;
D O I
10.1107/S2056989022006338
中图分类号
O7 [晶体学];
学科分类号
0702 ; 070205 ; 0703 ; 080501 ;
摘要
The isostructural compounds caesium decasodium tetrazirconium nonaarsenate, CsNa10Zr4(AsO4)(9), and caesium decasodium tetrahafnium nonaarsenate, CsNa10Hf4(AsO4)(9), arose as unexpected single-crystal products from the reactions of Na2CO3, MO2 (M = Zr, Hf) and As2O5 in a eutectic flux of NaCl and CsCl. They consist of MO6 octahedra and AsO4 tetrahedra sharing vertices to generate three-dimensional polyhedral networks encapsulating the caesium and sodium ions. The MO6 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. The Cs+ ion adopts a squashed octahedral geometry and the coordination polyhedra of the partially occupied sodium ions are variously trigonal bipyramidal, tetrahedral, square pyramidal and trigonal pyramidal. Site symmetries: Cs (3) over bar; M 3; As 1 and 2; O 1; Na 1, 2 and 3. The M = Zr crystal was refined as an obverse/reverse rhombohedral twin.
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页码:737 / +
页数:14
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