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EN
Two novel vic-dioxime, 1,2-dihydroxyimino-1-p-tolyl-3-aza-6-imidazole heptane (L1H2) and N-(ethyl-4-amino-1-piperidine carboxylate)-p-tolylglyoxime (L2H2) were prepared by the reaction of anti-p-tolylchloroglyoxime with 1-(3-aminopropyl)imidazole and ethyl-4-amino-1-piperidine carboxylate in absolute THF. Mononuclear complexes with a metal-ligand ratio of 1:2 were prepared using Co(II), Cu(II) and Ni(II) salts. The ligands and their Co(II), Cu(II) and Ni(II) com plexes were characterized by elemental analyses, FT-IR, UV-Vis, 1H-NMR and 13C-NMR and magnetic susceptibility measurements. The electrochemical behaviour of the complexes was investi ated by cyclic voltammetry in dimethylsulfoxide. All metal complexes showed metal centered quasi reversible one-electron redox processes. How ever, metal complexes of the L2H2 ligand also ex hibited ligand based irreversible redox waves.
EN
Several mononuclear Ni(II) and Co(II) complexes of bidentate salicylaldimines (LxH), derived from 3,5-di-tert-butyl-2-hydroxybenzaldehyde with biologically active amines [1-(3-aminopropyl)imidazole, 4-(3-aminopropyl)morpholine, 1-(3-aminopropyl)-2-pyrrolidinone], have been synthesized. The complexes have been characterized by FT-IR, UV-vis, MS, 1H-NMR and 13C-NMR, magnetic susceptibility measurements, thermogravimetric analyses (TGA) and electrochemistry. As a result of thermal analyses, Co(L3)2 has highest thermal stability of the complexes, whereas the smallest one has Ni(L2)2. Electrochemical experiments indicated that Ni(II) and Co(II) complexes show quasi reversible reduction to Ni(I) and Co(I), respectively.
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