Synthesis and Characterization of Water Stable Uranyl(V) Complexes
The importance of uranyl(V) (UO2+) species associated with environmental and geologic applications is becoming increasingly evident, but the tendency of the uranyl(V) cation to disproportionate in water has prevented the isolation of stable complexes. Here we demonstrate that in the presence of the...
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Veröffentlicht in: | Angewandte Chemie International Edition 2021-04, Vol.60 (15), p.8227-8235 |
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Sprache: | eng |
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Zusammenfassung: | The importance of uranyl(V) (UO2+) species associated with environmental and geologic applications is becoming increasingly evident, but the tendency of the uranyl(V) cation to disproportionate in water has prevented the isolation of stable complexes. Here we demonstrate that in the presence of the tridentate complexing dipicolinate (dpa2−), a ligand highly abundant in soil, the uranyl(V) species can be stabilized and isolated in anoxic basic water. Stable uranyl(V) dipicolinate complexes are readily formed from the reduction of the uranyl(VI) analogue both in organic solution and in basic water, and their solution and solid‐state structure were determined. A bis‐dpa UVO2+ complex was obtained from water at pH 10, while at higher pH values, a trinuclear mono‐dpa cation‐cation complex was isolated. These results present the second ever isolated water stable uranyl(V) complex. Moreover, we demonstrate that dipicolinate complexes of UVIO22+, UVO2+ and UIV are strongly luminescent with a signature characteristic of each oxidation state. This provides unique examples of luminescent UV and UIV compounds.
The tridentate dipicolinate ligand dpa2−, allowed to stabilize and isolate mononuclear and trinuclear uranyl(V) species in anoxic basic water providing the second example ever isolated of a water stable uranyl(V) and further demonstrating the environmental relevance of UV. The uranyl(VI), uranyl(V) and UIV dipicolinate complexes show very different measurable luminescent spectra characteristic of the uranium oxidation state. |
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ISSN: | 1433-7851 1521-3773 |
DOI: | 10.1002/anie.202016123 |