The synthesis and characterisation of two new iron thioantimonates:: [Fe(en)3]2Sb2S5•0.55H2O and [Fe(en)3]2Sb4S8

被引:36
作者
Lees, RJE
Powell, AV [1 ]
Chippindale, AM
机构
[1] Heriot Watt Univ, Dept Chem, Edinburgh EH14 4AS, Midlothian, Scotland
[2] Univ Reading, Sch Chem, Reading RG6 6AD, Berks, England
基金
英国工程与自然科学研究理事会;
关键词
thioantimonate; solvothermal synthesis; crystal structure; X-ray diffraction;
D O I
10.1016/j.poly.2005.06.017
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Two new iron thioantimonates, [Fe(en)(3)](2)Sb2S5 (.) 0.55H(2)O (1) and [Fe(en)(3)](2)Sb4S8 (2). were synthesised under solvothermal conditions from the reactions of Sb2S3, FeCl2 and S in the presence of ethylenediamine at 413 and 438 K, respectively. The products were characterised by single-crystal X-ray diffraction, elemental analysis and SQUID magnetometry. Compound 1 is unusual in containing isolated Sb2S54- anions formed from two corner-sharing SbS33- trigonal pyramids. These units are arranged in rippled layers, 4 A apart, parallel to the bc-plane. Octahedrally coordinated [Fe(en)(3)](2+) cations lie in depressions within these anionic layers. In compound (2), repeated corner linking of SbS33- trigonal pyramids generates SbS2- chains, which may be considered as a polymerised form of the Sb2S54- anions in 1. The SbS2- chains are separated by [Fe(en)(3)](2+) cations. In both compounds, there is an extensive network of hydrogen bonds between the nitrogen atoms of the ethylenediamine ligands and the sulfur atoms of the anions and, in the case of 1, the uncoordinated water molecule. (c) 2005 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1941 / 1948
页数:8
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