Pentavalent uranyl complexes

被引:196
作者
Arnold, Polly L. [1 ]
Love, Jason B. [1 ]
Patel, Dipti [1 ]
机构
[1] Univ Edinburgh, Sch Chem, Edinburgh EH9 3JJ, Midlothian, Scotland
基金
英国工程与自然科学研究理事会;
关键词
Uranyl; Uranium; Pentavalent; Disproportionation; Metal oxo; Multiple bonding; Cation-cation interactions; ELECTRONIC-STRUCTURE; UNCONVENTIONAL SUPERCONDUCTIVITY; COORDINATION CHEMISTRY; CRYSTAL-STRUCTURE; REDOX ENERGETICS; OXIDATION-STATE; URANIUM; REDUCTION; ION; MECHANISM;
D O I
10.1016/j.ccr.2009.03.014
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The uranyl dication, [UO2](2+), is the most prevalent and most thermodynamically stable form of uranium and is a soluble and problematic environmental contaminant. It is also extraordinarily chemically robust due to the strongly covalent trans-UO2 bonding. In contrast, the pentavalent uranyl cation [UO2](+) is unstable in an aqueous environment with respect to disproportionation into tetravalent uranium species and [UO2](2+). Aside from fundamental interest, an understanding of the pentavalent [UO2](+) cation is desirable since it is important environmentally as a key intermediate in the precipitation of uranium from groundwater. In the last 2 years, the use of anaerobic coordination chemistry techniques and organometallic reagents has allowed the isolation of a few kinetically inert complexes containing the f(1) [UO2](+) cation. The synthesis and characterisation of these, and the insight they give into subsequent reactivity of the trans-UO2 unit, is discussed in this review. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:1973 / 1978
页数:6
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