The novel Schiff base ligand, 4-methoxysalicyliden-p-aminoacetophenoneoxime (LH) was synthesized starting from p-aminoacetophenoneoxime and 4-methoxysalicylaldehyde. Mononuclear cobalt(II), copper(II) and zinc(II) complexes of the ligand have been prepared by using Co(II), Cu(II) and Zn(II) salt with a metal to ligand ratio of 1:2. The structures of the ligand and its complexes were identified by using elemental analyses, IR, 1H- and 13C-NMR spectra, magnetic susceptibility measurements, UV spectra and thermogravimetric analyses (TGA).
The interactions of Co(II) with a group of diastereoisomeric dipeptides containing a side chain with the aromatic phenyl ring have been studied in aqueous solution, both under inert atmosphere and in the presence of dioxygen. An effect of stereoselectivity has been observed in the metal promoted deprotonations, examined by glass electrode potentiometry and correlated with the results of UV/Vis spectroscopy. The kinetics of oxygenation were studied by the stopped flow method and related to the potentiometric results.
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In this work the selective transport of cobalt(II) and lithium(I) ions from aqueous chloride solutions through polymer inclusion membranes (PIMs) is presented. Triisooctylamine (TIOA) has been applied as the ion carrier in membrane. The effects of various parameters on the transport of Co(II) and Li(I) were studied. The obtained results show that Co(II) ions were effectively removed from source phase through PIM containing 32 wt.% TIOA, 22 wt.% CTA (cellulose triacetate) and 46 wt.% ONPOE (o-nitrophenyl octyl ether) or ONPPE (o-nitrophenyl pentyl ether) into deionized water as the receiving phase. The results indicate that there is a possibility of polymer inclusion membranes application to recover Co(II) and Li(I) from aqueous chloride solutions
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In this study, palladium-modified nickel foam substrate was applied to examine ethanol oxidation reaction (EOR) in 0.1 The transport of cobalt(II), nickel(II), copper(II), and zinc(II) ions from chloride solutions across polymer inclusion membranes (PIMs), which 1-heptylimidazole (1̲) or 1-heptyl-2-methylimidazole (2̲) or 1-heptyl-4-methylimidazole (3̲) as the ion carrier was reported. The steric effect for carriers 2̲and 3̲decreases the transport of all ions except Cu(II). The initial fl uxes of metal ions transport across PIMs with the 1̲- 2̲decrease in the sequence: Cu(II) > Zn(II) > Co(II) > Ni(II), whereas for 3 they were Cu(II) > Zn(II) > Ni(II) > Co(II). The highest recovery values were obtained for Cu(II), this being 99 and 85% for carrier 1̲and 2̲, respectively. In both membranes the degree of deposition of the Zn(II) ions was comparable. Zn(II), Co(II) and Cd(II) ions, which form complexes with coordination numbers 4 and 6, are more easily recovered with the use of carriers 2̲and 3̲. Ni(II) ions, which form complexes with coordination number 6 only, practically remain in the feeding phase. PIMs with alkylimidazoles were characterized by non-contact atomic force microscopy.
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