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Updated: Jul 22, 2026

Activating Molecules, Ions, and Solid Particles with Acoustic Cavitation
Published on: April 11, 2014
Uranium halide complexes in ionic liquids: an electrochemical and structural study
Maggel Deetlefs1, Charles L Hussey, Thamer J Mohammed
1QUILL Centre, David Keir Building, Stranmillis Road, Queen's University of Belfast, Belfast, Northern Ireland, UK BT9 5AG. quill@qub.ac.uk
Abstract:
The electrochemistry of the salts, [emim]2[UBr6] and [emim]2[UO2Br4] ([emim] = 1-ethyl-3-methylimidazolium), has been investigated in both a basic and an acidic bromoaluminate(III) ionic liquid. In the basic ionic liquid, the hexabromo salt undergoes a one-electron reversible reduction process at a stationary glassy carbon disc electrode, while the tetrabromodioxo salt was reduced to a uranium(IV) species by an irreversible two-electron process with the simultaneous transfer of oxide to the ionic liquid. On the other hand, dissolution of either of the salts in an acidic bromoaluminate(III) ionic liquid resulted in the formation of the same electroactive species. The solid state structures of the uranium chloride salts, [emim]2[UCl6] and [emim]2[UO2Cl4], have previously been reported, but have now been re-evaluated using a new statistical model developed in our group, to determine the presence or absence of weak hydrogen bonding interactions in the crystalline state.
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