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Synthesis, structure, and solvent-extraction properties of tridentate oxime ligands and their cobalt(II), nickel(II), copper(II), zinc(II) complexes

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dc.creator KARİPCİN, Fatma
dc.creator ARABALI, Filiz
dc.creator CENGİZ, Mustafa
dc.creator Dede, Bülent
dc.date 2010-01-31T22:00:00Z
dc.date.accessioned 2020-10-06T09:18:50Z
dc.date.available 2020-10-06T09:18:50Z
dc.identifier 09f25b06-b9a7-4020-86c8-74137a9b8b65
dc.identifier 10.2478/s11696-009-0095-6
dc.identifier https://avesis.sdu.edu.tr/publication/details/09f25b06-b9a7-4020-86c8-74137a9b8b65/oai
dc.identifier.uri http://acikerisim.sdu.edu.tr/xmlui/handle/123456789/52813
dc.description Synthesis of four different types of ligands Ar[COC(NOH)R] (n) (Ar = biphenyl, n = 1, HL1; Ar = biphenyl, n = 2, H2L2; Ar = diphenylmethane, n = 1, HL3; Ar = diphenylmethane, n = 2, H2L4; R = furfurylamine in all ligands) and their dinuclear Co2+, Ni2+, Cu2+, and Zn2+ complexes is reported herein. These compounds were characterized by elemental analysis, ICP-OES, FT-IR spectra, and magnetic susceptibility measurements. The ligands were further characterized by H-1 NMR. The results suggest that dinuclear complexes of HL1 and HL3 have a metal to ligand mole ratio of 2: 2 and dinuclear complexes H2L2 and H2L4 have a metal to ligand mole ratio of 2: 1. Square pyramidal or octahedral structures are proposed for complexes of oxime ligands. Furthermore, extraction abilities of the four ligands were also evaluated in chloroform using selected transition metal picrates such as Mn2+, Co2+, Ni2+, Cu2+, Zn2+, Cd2+, Hg2+, Pb2+. The ligands show strong binding ability towards Hg2+ and Cu2+ ions.
dc.language eng
dc.rights info:eu-repo/semantics/closedAccess
dc.title Synthesis, structure, and solvent-extraction properties of tridentate oxime ligands and their cobalt(II), nickel(II), copper(II), zinc(II) complexes
dc.type info:eu-repo/semantics/article


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