SYNTHESIS AND CRYSTAL-STRUCTURES OF K5SE3, CS5TE3 AND CS2TE

被引:39
作者
SCHEWEMILLER, I [1 ]
BOTTCHER, P [1 ]
机构
[1] UNIV DUSSELDORF,INST ANORGAN CHEM & STRUKTURCHEM 2,W-4000 DUSSELDORF 1,GERMANY
来源
ZEITSCHRIFT FUR KRISTALLOGRAPHIE | 1991年 / 196卷 / 1-4期
关键词
ALKALI METAL CHALCOGENIDES; POLYCHALCOGENIDES; W5SI3-TYPE;
D O I
10.1524/zkri.1991.196.1-4.137
中图分类号
O7 [晶体学];
学科分类号
0702 ; 070205 ; 0703 ; 080501 ;
摘要
We describe the syntheses and the crystal structures of K5Se3, Cs5Te3, and Cs2Te. The substructure of low-temperature-(LT-)K5Se3 was solved by single crystal X-ray analysis (a = 18.289(3) angstrom, b = 5.861(2) angstrom, c = 12.988(2) angstrom, beta = 134.82(1)-degrees, Z = 4, C2/m); it is a monoclinic distortion of the K5Te3-type, which itself is closely related to the W5Si3-type. Furthermore, we propose a model for the incommensurate superstructure of LT-K5Se3, which reproduces the main features of the observed satellites. By X-ray powder diffraction we determined the structures of high-temperature-(HT)-K5Se3 (K5Te3-type: cell constants at 200-degrees-C: a = 13.097(1) angstrom, c = 5.882(1) angstrom, Z = 4, 14/m), Cs5Te3 (LT-K5Se3-type: a = 21.11(2) angstrom, b = 6.655(1) angstrom, c = 15.07(1) angstrom, beta = 134.53(5)-degrees, Z = 4, C2/m), and Cs2Te (PbCl2-type: a = 9.109(2) angstrom, b = 5.871(1) angstrom, c = 11.494(2) angstrom, Z = 4, Pnma), and, with additional thermoanalytic methods, we investigated the phase transition LT-K5Se3 reversible HT-K5Se3.
引用
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页码:137 / 151
页数:15
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