Protonation constants of some N-substituted amidoximes in a 50% ethanol-water mixture (v/v)

dc.contributor.authorAkay, Mehmet Abdülkadir
dc.contributor.authorKılıç, Esma
dc.contributor.departmentFen Fakültesitr_TR
dc.date.accessioned2019-07-02T08:12:24Z
dc.date.available2019-07-02T08:12:24Z
dc.date.issued2000
dc.description.abstractThe stoichiometric protonation constants of some N-substituted amidoximes have been determined potentiometrically in a 50% ethanol-water mixture (v/v) at 25 degrees C and at constant ionic strength. A calculation was performed using a PC software. The variation of the protonation constants of these compounds was interpreted on the basis of structural effects exposed by the substituents and main skeleton.tr_TR
dc.description.indexWos
dc.identifier.endpage827tr_TR
dc.identifier.issue08tr_TR
dc.identifier.other10.2116/analsci.16.825
dc.identifier.startpage825tr_TR
dc.identifier.urihttp://hdl.handle.net/20.500.12575/67162
dc.identifier.volume16tr_TR
dc.language.isoentr_TR
dc.relation.indexWOStr_TR
dc.relation.journalAnalytical Sciencestr_TR
dc.subjectBond-dissociation energies; equilibrium acidities; structural-changes; salicylideneanilinestr_TR
dc.titleProtonation constants of some N-substituted amidoximes in a 50% ethanol-water mixture (v/v)tr_TR
dc.typeArticle

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