4.8 Review

Pentavalent uranyl complexes

Journal

COORDINATION CHEMISTRY REVIEWS
Volume 253, Issue 15-16, Pages 1973-1978

Publisher

ELSEVIER SCIENCE SA
DOI: 10.1016/j.ccr.2009.03.014

Keywords

Uranyl; Uranium; Pentavalent; Disproportionation; Metal oxo; Multiple bonding; Cation-cation interactions

Funding

  1. Engineering and Physical Sciences Research Council [EP/G038945/1] Funding Source: researchfish
  2. EPSRC [EP/G038945/1] Funding Source: UKRI

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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.

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