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Neutral (bis-beta-diketonato) iron(III), cobalt(II), nickel(II), copper(II) and zinc(II) metallocycles: structural, electrochemical and solvent extraction studies
Authors:Clegg Jack K  Bray David J  Gloe Kerstin  Gloe Karsten  Hayter Michael J  Jolliffe Katrina A  Lawrance Geoffrey A  Meehan George V  McMurtrie John C  Lindoy Leonard F  Wenzel Marco
Institution:Centre for Heavy Metals Research, School of Chemistry, University of Sydney, NSW 2006, Australia.
Abstract:Neutral dimeric metallocyclic complexes of type M(2)(L(1))(2)B(n)] (where M = cobalt(II), nickel(II) and zinc(II), L(1) is the doubly deprotonated form of a 1,3-aryl linked bis-beta-diketone ligand of type 1,3-bis(RC(O)CH(2)C(O))C(6)H(4) (R=Me, n-Pr, t-Bu) and B is pyridine (Py) or 4-ethylpyridine (EtPy)) have been synthesised, adding to similar complexes already reported for copper(II). New lipophilic ligand derivatives with R = octyl or nonyl were also prepared for use in solvent extraction experiments. Structural, electrochemical and solvent extraction investigations of selected metal complex systems from the above series are reported, with the X-ray structures of Co(2)(L(1))(2)(Py)(4)] x 2.25CHCl(3) x 0.5H(2)O (R=Pr), Co(2)(L(1))(2)(EtPy)(4)] (R=t-Bu), Ni(2)(L(1))(2)(EtPy)(4)] (R=t-Bu), Zn(2)(L(1))(2)(EtPy)(2)] (R=Me) and Zn(2)(L(1))(2)(EtPy)(4)] (R=t-Bu) being presented. The electrochemistry of H(2)L(1) (R=t-Bu) and of Fe(2)(L(1))(3)], Co(2)(L(1))(2)(Py)(4)], Ni(2)(L(1))(2)(Py)(4)], Cu(2)(L(1))(2)] and Zn(2)(L(1))(2)(Py)(2)] has been examined. Oxidative processes for the complexes are dominantly irreversible, but several examples of quasireversible behaviour were observed and support the assignment of an anodic process, seen between +1.0 and +1.6 V, as a metal-centred oxidation. The reduction processes for the respective metal complexes are not simple, and irreversible in most cases. Solvent extraction studies (water/chloroform) involving variable concentrations of metal, bis-beta-diketone and heterocyclic base have been performed for cobalt(II) and zinc(II) using a radiotracer technique to probe the stoichiometries of the extracted species in each case. Synergism was observed when 4-ethylpyridine was added to the bis-beta-diketone ligand in the chloroform phase. Competitive extraction studies show a clear uptake preference for copper(II) over cobalt(II), nickel(II), zinc(II) and cadmium(II).
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