Tricaesium tris(oxalato-κ2O1,O2)chromate(III) dihydrate

被引:5
|
作者
Martin, Lee [1 ]
Christian, Anthony [1 ]
Akutsu, Hiroki [2 ]
机构
[1] Nottingham Trent Univ, Sch Sci & Technol, Nottingham NG11 8NS, England
[2] Univ Hyogo, Grad Sch Mat Sci, Kamigori, Hyogo 6781297, Japan
关键词
CHARGE-TRANSFER SALTS;
D O I
10.1107/S0108270110014861
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The title compound, Cs-3[Cr(C2O4)(3)]center dot 2H(2)O, has been synthesized for the first time and the spatial arrangement of the cations and anions is compared with those of the other members of the alkali metal series. The structure is built up of alternating layers of either the d or l enantiomers of [Cr(oxalate)(3)](3-). Of note is that the distribution of the [Cr(oxalate)(3)](3-) enantiomers in the Li+, K+ and Rb+ tris(oxalato)chromates differs from those of the Na+ and Cs+ tris(oxalato) chromates, and also differs within the corresponding BEDT-TTF [bis(ethylenedithio)tetrathiafulvalene] conducting salts. The use of tris(oxalato) chromate anions in the crystal engineering of BEDT-TTF salts is discussed, wherein the salts can be paramagnetic superconductors, semiconductors or metallic proton conductors, depending on whether the counter-cation is NH4+, H3O+, Li+, Na+, K+, Rb+ or Cs+. These materials can also be superconducting or semiconducting, depending on the spatial distribution of the d and l enantiomers of [Cr(oxalate)(3)](3-).
引用
收藏
页码:M157 / M159
页数:3
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