Synthesis and complex formation of substituted amino-2-naphthylglyoximes of unsymmetrical vic-dioximes

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dc.contributor.authorYildirim S.
dc.contributor.authorPekacar A.I.
dc.contributor.authorUçan M.
dc.date.accessioned2019-08-01T13:38:39Z
dc.date.available2019-08-01T13:38:39Z
dc.date.issued2003
dc.departmentNiğde ÖHÜ
dc.description.abstractanti-2-Naphthylchloroglyoxime has been synthesized by chlorination of anti-2-naphthylglyoxime. Reaction with aryl-or arylalkylamines in EtOH between 15°C and 20°C gives unsymmetrical vic-dioximes, namely, anilino-2-naphthylglyoxime (L1H2), benzylamino-2-naphthylglyoxime (L2H2), p-toluidino-2-naphthylglyoxime (L3H2) 1-naphthylamino-2-naphthylglyoxime (L4H2). The Ni(II) and Cu(II) complexes of these ligands are square-planar while the Co(II) complexes are octahedral with water molecules as axial ligands. 1H NMR, IR and elemental analyses data of the complexes and ligands are discussed.
dc.identifier.doi10.1081/SIM-120021654
dc.identifier.endpage882
dc.identifier.issn0094-5714
dc.identifier.issue5
dc.identifier.scopus2-s2.0-0038449332
dc.identifier.scopusqualityN/A
dc.identifier.startpage873
dc.identifier.urihttps://dx.doi.org/10.1081/SIM-120021654
dc.identifier.urihttps://hdl.handle.net/11480/1338
dc.identifier.volume33
dc.identifier.wosWOS:000183374700010
dc.identifier.wosqualityQ4
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.institutionauthor[0-Belirlenecek]
dc.language.isoen
dc.relation.ispartofSynthesis and Reactivity in Inorganic and Metal-Organic Chemistry
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.titleSynthesis and complex formation of substituted amino-2-naphthylglyoximes of unsymmetrical vic-dioximes
dc.typeArticle

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