Deprotonation of salicylic acid and 5-nitrosalicylic acid in aqueous solutions of ethanol

The protonation constant values of two hydroxybenzoic acids (salicylic and 5-nitrosalicylic acid) were studied in some water-ethanol solutions using spectrophotometric and potentiometric methods at 25°C and in an ionic strength of 0.1 M sodium perchlorate. The results indicated that the pKa valu...

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Main Authors: Faraji Mohammad, Farajtabar Ali, Gharib Farrokh, Ghasemnejad-Borsa Hassan
Format: Article
Language:English
Published: Serbian Chemical Society 2011-01-01
Series:Journal of the Serbian Chemical Society
Subjects:
Online Access:http://www.doiserbia.nb.rs/img/doi/0352-5139/2011/0352-51391100129F.pdf
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author Faraji Mohammad
Farajtabar Ali
Gharib Farrokh
Ghasemnejad-Borsa Hassan
author_facet Faraji Mohammad
Farajtabar Ali
Gharib Farrokh
Ghasemnejad-Borsa Hassan
author_sort Faraji Mohammad
collection DOAJ
description The protonation constant values of two hydroxybenzoic acids (salicylic and 5-nitrosalicylic acid) were studied in some water-ethanol solutions using spectrophotometric and potentiometric methods at 25°C and in an ionic strength of 0.1 M sodium perchlorate. The results indicated that the pKa values increase with increasing proportion of ethanol in mixed solvent. The dependence of the protonation constants on the variation of the solvent were correlated by the dielectric constants of the media. Furthermore, for a better understanding of the solvent influence, the obtained results were explained in terms of the Kamlet-Taft parameters α (hydrogen-bond donor acidity), π
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spelling doaj.art-7083f38a4f4249a2bf546c8ac044ea942022-12-21T19:10:28ZengSerbian Chemical SocietyJournal of the Serbian Chemical Society0352-51392011-01-0176111455146310.2298/JSC100506129FDeprotonation of salicylic acid and 5-nitrosalicylic acid in aqueous solutions of ethanolFaraji MohammadFarajtabar AliGharib FarrokhGhasemnejad-Borsa HassanThe protonation constant values of two hydroxybenzoic acids (salicylic and 5-nitrosalicylic acid) were studied in some water-ethanol solutions using spectrophotometric and potentiometric methods at 25°C and in an ionic strength of 0.1 M sodium perchlorate. The results indicated that the pKa values increase with increasing proportion of ethanol in mixed solvent. The dependence of the protonation constants on the variation of the solvent were correlated by the dielectric constants of the media. Furthermore, for a better understanding of the solvent influence, the obtained results were explained in terms of the Kamlet-Taft parameters α (hydrogen-bond donor acidity), πhttp://www.doiserbia.nb.rs/img/doi/0352-5139/2011/0352-51391100129F.pdfpKahydroxybenzoic acidsBinary mixturesSolvent effects
spellingShingle Faraji Mohammad
Farajtabar Ali
Gharib Farrokh
Ghasemnejad-Borsa Hassan
Deprotonation of salicylic acid and 5-nitrosalicylic acid in aqueous solutions of ethanol
Journal of the Serbian Chemical Society
pKa
hydroxybenzoic acids
Binary mixtures
Solvent effects
title Deprotonation of salicylic acid and 5-nitrosalicylic acid in aqueous solutions of ethanol
title_full Deprotonation of salicylic acid and 5-nitrosalicylic acid in aqueous solutions of ethanol
title_fullStr Deprotonation of salicylic acid and 5-nitrosalicylic acid in aqueous solutions of ethanol
title_full_unstemmed Deprotonation of salicylic acid and 5-nitrosalicylic acid in aqueous solutions of ethanol
title_short Deprotonation of salicylic acid and 5-nitrosalicylic acid in aqueous solutions of ethanol
title_sort deprotonation of salicylic acid and 5 nitrosalicylic acid in aqueous solutions of ethanol
topic pKa
hydroxybenzoic acids
Binary mixtures
Solvent effects
url http://www.doiserbia.nb.rs/img/doi/0352-5139/2011/0352-51391100129F.pdf
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