Coordination geometry of Cr(VI) species: Structural and spectroscopic characteristics

被引:44
作者
Cieslak-Golonka, M [1 ]
Daszkiewicz, M [1 ]
机构
[1] Wroclaw Univ Technol, Inst Organ Chem & Met Rare Elements, PL-50370 Wroclaw, Poland
关键词
chromium(VI); coordination geometry; intermediates; structure; spectroscopy;
D O I
10.1016/j.ccr.2005.03.029
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
In this review, the speciation of chromium(VI) entities, the key to understanding the further redox processes related to this ion, is presented and discussed. Two possible modes of Cr(VI) binding, i.e. as a centre of coordination and as a ligand, have been characterized. In contrast to the gas and solid-state phases, where coordination number four is generally preserved, the Cr(VI) coordination sphere may be more flexible and chromium(VI) forms can even be seven-coordinate in solution. In the solid state, the pseudotetrahedral stereochemistry of the [CrO4](2-) species does not exclude versatility of its coordination modes, e.g. monodentate, polymeric bridging, bidentate, chelate, etc. The difficulties and various problems associated with structural aspects of Cr(VI) forms, mainly in relation to their spectroscopic properties, are shown. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:2391 / 2407
页数:17
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