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离子液体中的卤化铀配合物:电化学与结构研究

Uranium halide complexes in ionic liquids: an electrochemical and structural study.

作者信息

Deetlefs Maggel, Hussey Charles L, Mohammed Thamer J, Seddon Kenneth R, van den Berg Jan-Albert, Zora Jalal A

机构信息

QUILL Centre, David Keir Building, Stranmillis Road, Queen's University of Belfast, Belfast, Northern Ireland, UK BT9 5AG.

出版信息

Dalton Trans. 2006 May 21(19):2334-41. doi: 10.1039/b512212k. Epub 2006 Feb 22.

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.

摘要

已在碱性和酸性溴化铝(III)离子液体中研究了盐[emim]2[UBr6]和[emim]2[UO2Br4]([emim] = 1-乙基-3-甲基咪唑鎓)的电化学性质。在碱性离子液体中,六溴盐在固定的玻碳圆盘电极上经历单电子可逆还原过程,而四溴二氧盐通过不可逆的双电子过程被还原为铀(IV)物种,同时氧化物转移到离子液体中。另一方面,将任何一种盐溶解在酸性溴化铝(III)离子液体中都会导致形成相同的电活性物种。铀氯化物盐[emim]2[UCl6]和[emim]2[UO2Cl4]的固态结构此前已有报道,但现在已使用我们小组开发的新统计模型重新评估,以确定晶体状态下是否存在弱氢键相互作用。

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