Abstract

Three new vic-dioxime: N -(2-methyl-2-butylamine)-anti-p-tolylglyoxime (L1H2), N -(4-amino-2,2,6,6-tetramethylpiperidine)-anti-p-tolylglyoxime (L2H2) and N,N′-(4-amino-2,2,6,6-tetramethylpiperidine)-anti-glyoxime (L3H2) were prepared by the reaction of anti-p-tolylchloroglyoxime and anti-dichloroglyoxime with 2-methyl-2-butylamine and 4-amino-2,2,6,6-tetramethylpiperidine in absolute THF at −15°C. Mononuclear metal complexes with a metal-ligand ratio of 1:2 were prepared using Cu(II), Ni(II) and Co(II) salts. FT-IR spectra show that the ligands act in a tetradentate manner and coordinates N4 donor groups of ligands to Cu(II), Ni(II) and Co(II) ions. The Cu(II) complexes of these ligands are proposed to be square-planar; the Ni(II) and Co(II) complexes are proposed to be octahedral with two water molecules as axial ligands. The ligands and their metal complexes were characterized by elemental analyses, Ft-IR, UV-Vis, 1H and 13C-NMR spectra, magnetic susceptibility measurements and cyclic voltammetry. The electrochemical behavior of the Ni(II), Co(II) and Cu(II) complexes was investigated by cyclic voltammetry in DMSO as well.

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