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dc.contributor.authorCakir, S
dc.contributor.authorBicer, E
dc.contributor.authorEleman, A
dc.date.accessioned2020-06-21T15:49:24Z
dc.date.available2020-06-21T15:49:24Z
dc.date.issued2001
dc.identifier.issn0340-4285
dc.identifier.urihttps://doi.org/10.1023/A:1007119907894
dc.identifier.urihttps://hdl.handle.net/20.500.12712/22224
dc.descriptionWOS: 000165089500016en_US
dc.description.abstractTwo Cu-II complexes of the type [Cu(L-1)(L-2)] (where L-1 = tryptophanate or phenylalaninate; L-2 = cysteine thiolate) have been prepared and characterised, and their spectrophotometric and voltammetric behaviour has been investigated. The results obtained by means of FT-IR, e.s.r., u.v.-vis. spectroscopy and by voltammetry revealed the existence of two different [Cu(L-1)(L-2)] complexes. A significance decrease in the g(parallel to) value and, concomitantly, an increase in the d-d transition energy was observed when a mixed-ligand complex is present. The observed anisotropic g-values indicate the presence of Cu-II in a tetragonally distorted octahedral geometry. Formation of a mixed-ligand copper complex can be considered as a type of synergism in the presence of cysteine. The redox state Cu-II or Cu-I of copper in the Cu(L-2) complex depends on the analysing conditions, i.e., cysteine forms a (CuI)-I-I complex under aerobic conditions and a Cu-I complex in anaerobic media. Tryptophan or phenylalanine is bound to Cu-II ions in the Cu(L-1) complexes.en_US
dc.language.isoengen_US
dc.publisherKluwer Academic Publen_US
dc.relation.isversionof10.1023/A:1007119907894en_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.titleSynthesis, spectroscopic and voltammetric studies of mixed-ligand copper(II) complexes of amino acidsen_US
dc.typearticleen_US
dc.contributor.departmentOMÜen_US
dc.identifier.volume26en_US
dc.identifier.issue01.Feben_US
dc.identifier.startpage89en_US
dc.identifier.endpage95en_US
dc.relation.journalTransition Metal Chemistryen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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