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dc.contributor.authorMacit, M
dc.contributor.authorBati, B
dc.contributor.authorOzdemir, M
dc.date.accessioned2020-06-21T11:31:51Z
dc.date.available2020-06-21T11:31:51Z
dc.date.issued1995
dc.identifier.issn0094-5714
dc.identifier.urihttps://doi.org/10.1080/15533179508014695
dc.identifier.urihttps://hdl.handle.net/20.500.12712/9904
dc.descriptionWOS: A1995TK45300012en_US
dc.description.abstractEight new substituted phenylamino and diaminoglyoximes; N-(3-methylphenyl)aminoglyoxime (MPAGH(2)), N-(2,6-dimethylphenyl)aminoglyoxime (DMPAGH(2)), N-(2-chloro-4-methylphenyl)aminoglyoxime (CMPAGH(2)), N-(2,4-dichlorophenyl)aminoglyoxime (DCPAGH(2)), N,N'-bis-(3-methylphenyl)diaminoglyoxime (BMPAGH(2)), N,N'-bis-(2,6-dimethylphenyl)diaminoglyoxime (BDMPAGH(2)), N,N'-bis(2-chloro-4-methylphenyl)diaminoglyoxime (BCMPAGH(2)), and N,N'-bis(2,4-dichlorophenyl)diaminoglyoxime (BDCPAGH(2)) have been synthesized by the reactions of anti-chloroglyoxime and dichloroglyoxime with substituted aromatic amines in absolute ethanol. All these dioximes are in the anti- form according to IR and H-1 NMR spectral data. The Ni(ll), Cu(ll) and Co(ll) complexes of eight vic-dioximes have been prepared and their structures have been determined by using IR and UV-VIS spectral data acid elemental analyses.en_US
dc.language.isoengen_US
dc.publisherMarcel Dekker Incen_US
dc.relation.isversionof10.1080/15533179508014695en_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.titleSynthesis of eight new substituted phenylamino and diaminoglyoximes and their complexes with some transition metalsen_US
dc.typearticleen_US
dc.contributor.departmentOMÜen_US
dc.identifier.volume25en_US
dc.identifier.issue10en_US
dc.identifier.startpage1733en_US
dc.identifier.endpage1747en_US
dc.relation.journalSynthesis and Reactivity in Inorganic and Metal-Organic Chemistryen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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