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Solvent Effects on pK(a) values of Some Substituted Sulfonamides in Acetonitrile-Water Binary Mixtures by the UV-Spectroscopy Method

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dc.creator Altun, Yueksel
dc.creator Alsancak, Gueleren
dc.creator Beltran, Jose L.
dc.creator Sanli, Senem
dc.creator Sanli, Nurullah
dc.date 2009-11-01T01:00:00Z
dc.date.accessioned 2021-12-03T12:02:36Z
dc.date.available 2021-12-03T12:02:36Z
dc.identifier ca303160-6f1d-4c45-b487-6b807ea828cc
dc.identifier 10.1021/je9000813
dc.identifier https://avesis.sdu.edu.tr/publication/details/ca303160-6f1d-4c45-b487-6b807ea828cc/oai
dc.identifier.uri http://acikerisim.sdu.edu.tr/xmlui/handle/123456789/94865
dc.description The examination of the dissociation constants of sulfonamides is essential in drug-design studies and in explaining the biopharmaceutical properties of substances. The dissociation constants of ten common human and veterinary antibiotics, namely, sulfadiazine, sulfamerazine, sulfamethoxazole, sulfathiazole, sulfamonomethoxine, sulfamethoxypyridazine, sulfadimethoxine, sulfafurazole, sulfadoxine, and sulfaquinoxaline, in water and in 15 %, 23 %, and 30 % (v/v) acetonitrile-water mixtures were determined by a UV/pH titration method and correlated with the Kamlet and Taft solvatochromic parameters, pi*, alpha, and beta. Kamlet and Taft's general equation was reduced to two terms by combined factor analysis and target factor analysis in these mixtures: the independent term and polarity/polafizability pi*, which is a solvatochromic parameter. Further, the quasi-lattice quasi-chemical (QLQC) theory of preferential solvation has been applied to quantify the preferential solvation by water of electrolytes in acetonitrile-water mixtures.
dc.language eng
dc.rights info:eu-repo/semantics/closedAccess
dc.title Solvent Effects on pK(a) values of Some Substituted Sulfonamides in Acetonitrile-Water Binary Mixtures by the UV-Spectroscopy Method
dc.type info:eu-repo/semantics/article


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