Structural variations in metal complexes of a tertiary α-hydroxyoxime

Despite the long term interest in hydroxyoximes as metal ion extractants, there is a lack of information on the possible coordination modes these ligands can assume, particularly in concert with a co-ligand. This is pertinent to the use of these extractants in synergistic systems, where a combinatio...

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Bibliographic Details
Main Authors: D'Alessio, D., Lombardo, D., Vaughan, J., Skelton, B., Barnard, K., Ogden, Mark
Format: Journal Article
Published: Royal Society of Chemistry 2015
Online Access:http://hdl.handle.net/20.500.11937/37410
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Summary:Despite the long term interest in hydroxyoximes as metal ion extractants, there is a lack of information on the possible coordination modes these ligands can assume, particularly in concert with a co-ligand. This is pertinent to the use of these extractants in synergistic systems, where a combination of extractants can achieve commercially useful results. We report here the structures of some metal complexes (M = Mn, Co, Ni, Cu, and Zn) with (1-hydroxycyclohexyl)-phenyl ketone oxime. The results demonstrate that this ligand can support complexes ranging from mononuclear to trinuclear, in association with anionic and neutral co-ligands in some cases. While these results have been obtained in the solid state, they illustrate a range of possible species that may be formed in extractant solutions.