Akay, Mehmet AbdülkadirKılıç, Esma2019-07-022019-07-02200010.2116/analsci.16.825http://hdl.handle.net/20.500.12575/67162The 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.enBond-dissociation energies; equilibrium acidities; structural-changes; salicylideneanilinesProtonation constants of some N-substituted amidoximes in a 50% ethanol-water mixture (v/v)Article1608825827