作者: Michael Wachhold , William S. Sheldrick
关键词: Solid solution 、 Crystal structure 、 Atom 、 Crystallography 、 Isostructural 、 Structure (category theory) 、 Orthorhombic crystal system 、 Chemistry 、 Monoclinic crystal system 、 Caesium 、 Physical and Theoretical Chemistry 、 Inorganic chemistry 、 Materials Chemistry 、 Electronic, Optical and Magnetic Materials 、 Condensed matter physics 、 Ceramics and Composites
摘要: Abstract The methanolothermal reaction of Cs2CO3with Se in the presence Bi2Te3at 160°C yields two tellurium-poor mixed polychalcogenides general type Cs4TexSe16−x. Cs4TeSe15is isostructural with Cs4Se16and crystallizes orthorhombic space groupPbcmwitha=10.042(2),b=14.029(3),c=19.120(4) A,Z=4, andV=2693.6(10) A3. It contains discrete [TeSe15]4−anions, which a central Te atom is coordinated distorted square-planar manner by three Se2−5chains, one chelating. Cs2Te2Se6crystallizes monoclinic groupP21/cwitha=7.436(1),b=6.771(1),c=13.489(3) A,β=95.55(3)°,Z=2, andV=676.0(2) A3and Cs2Te8. If distances longer than 2.90 A are ignored, anionic structure may be described as [Te2Se6]2−chain atoms adopt third and sixth positions. Individual chains connected through Te···Se interactions lengths 2.922(2) 3.244(1) into sheets. When Sb2Te3is employed place Bi2Te3, Cs4[TeSe3]2·Te3Se3·1.5(Te3.21Se2.79) pyramidal [TeSe3]2−anions respectively ordered disordered TexSe6−xrings secondary bonds polymeric layers. Cs4Te9.74Se13.26crystallizes rhombohedral groupR 3 witha=b=12.022(2),c=44.072(9) A,Z=6, andV=5516(2)