Please use this identifier to cite or link to this item: http://hdl.handle.net/11452/26521
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dc.date.accessioned2022-05-18T08:56:43Z-
dc.date.available2022-05-18T08:56:43Z-
dc.date.issued2004-11-
dc.identifier.citationAksoy, M. S. ve Özer, U. (2004). “Equilibrium studies on chromium(III) complexes of salicylic acid and salicylic acid derivatives in aqueous solution”. Chemical and Pharmaceutical Bulletin, 52(11), 1280-1284.en_US
dc.identifier.issn0009-2363-
dc.identifier.urihttps://doi.org/10.1248/cpb.52.1280-
dc.identifier.urihttps://www.jstage.jst.go.jp/article/cpb/52/11/52_11_1280/_article-
dc.identifier.urihttp://hdl.handle.net/11452/26521-
dc.description.abstractThe complexes of chromium(III) ion formed by salicylic acid, SA(H2L), and its derivatives (H2L): 5-nitrosalicylic acid (5-NSA), 5-sulphosalicylic acid (5-SSA) were investigated by means of potentiometry and spectroscopy, at 25degreesC and in ionic strength of 0.1 m KNO3 and 0.1 m KCI, respectively. Over the acidic pH range, the coordination of Cr(III) ion to SA and its derivatives in 1:1 mole ratio occurs, CrL+ type complex is formed. In the excess of ligand, the coordination of the second ligand molecule is somewhat hindered; as a result CrL(HL) type complex occurs. Their existences were verified and their formation constants were determined. At near neutral pH, CrL(OH) and CrL(HL)(OH)(-) type hydroxo complexes formed by hydrolytic equilibria and their formation constants were also defined. The stabilities of Cr(III) complexes of SA and its derivatives decrease in the following order: SA>5-SSA>5-NSA. The formation constants of Cr(III) complexes of SA and its derivatives are in comparable ranges with the corresponding complexes of the 2,x-dihydroxybenzoic acid (2,x-DHBA) of Cr(III) ion. The stabilities of SA complexes for V(IV), Cr(III) and Fe(III) ions that have similar ionic radii, increase in the order VOLen_US
dc.language.isoenen_US
dc.publisherPharmaceutical Soc Japanen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.rightsAtıf Gayri Ticari Türetilemez 4.0 Uluslararasıtr_TR
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectPharmacology and pharmacyen_US
dc.subjectChemistryen_US
dc.subjectChromiumen_US
dc.subjectSalicylic aciden_US
dc.subjectSalicylic acid derivativeen_US
dc.subjectPotentiometryen_US
dc.subjectStability constanten_US
dc.subjectHydroxyaromatic ligandsen_US
dc.subjectStability constantsen_US
dc.subjectPhenolsen_US
dc.subjectAl(III)en_US
dc.subjectBindingen_US
dc.subject.meshChromiumen_US
dc.subject.meshHydrogen-ion concentrationen_US
dc.subject.meshSalicylatesen_US
dc.subject.meshSalicylic aciden_US
dc.subject.meshSolutionsen_US
dc.subject.meshWateren_US
dc.titleEquilibrium studies on chromium(III) complexes of salicylic acid and salicylic acid derivatives in aqueous solutionen_US
dc.typeArticleen_US
dc.identifier.wos000225154700003tr_TR
dc.identifier.scopus2-s2.0-19644365051tr_TR
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergitr_TR
dc.contributor.departmentUludağ Üniversitesi/Fen-Edebiyat Fakültesi/Kimya Bölümü.tr_TR
dc.identifier.startpage1280tr_TR
dc.identifier.endpage1284tr_TR
dc.identifier.volume52tr_TR
dc.identifier.issue11tr_TR
dc.relation.journalChemical and Pharmaceutical Bulletinen_US
dc.contributor.buuauthorAksoy, Mehmet Suat-
dc.contributor.buuauthorÖzer, Ulviye-
dc.identifier.pubmed15516746tr_TR
dc.subject.wosChemistry, medicinalen_US
dc.subject.wosChemistry, multidisciplinaryen_US
dc.subject.wosPharmacology and pharmacyen_US
dc.indexed.wosSCIEen_US
dc.indexed.scopusScopusen_US
dc.indexed.pubmedPubMeden_US
dc.wos.quartileQ3en_US
dc.wos.quartileQ2 (Chemistry, multidisciplinary)en_US
dc.contributor.scopusid8986297500tr_TR
dc.contributor.scopusid6601993613tr_TR
dc.subject.scopusBeryllium; Electrospray Ionization; Ligandsen_US
dc.subject.emtreeAcidityen_US
dc.subject.emtreeAlkalinityen_US
dc.subject.emtreeAqueous solutionen_US
dc.subject.emtreeArticleen_US
dc.subject.emtreeDrug bindingen_US
dc.subject.emtreeDrug stabilityen_US
dc.subject.emtreeInsulin releaseen_US
dc.subject.emtreeIonic strengthen_US
dc.subject.emtreePh measurementen_US
dc.subject.emtreePotentiometric titrationen_US
dc.subject.emtreeChemistryen_US
dc.subject.emtreepHen_US
dc.subject.emtreeSolution and solubilityen_US
dc.subject.emtree5 nitrosalicylic aciden_US
dc.subject.emtreeBenzoic acid derivativeen_US
dc.subject.emtreeChromium derivativeen_US
dc.subject.emtreeInsulinen_US
dc.subject.emtreePlasma proteinen_US
dc.subject.emtreeSalicylic aciden_US
dc.subject.emtreeSalicylic acid derivativeen_US
dc.subject.emtreeSulfosalicylic aciden_US
dc.subject.emtreeTransferrinen_US
dc.subject.emtree5 nitroso-salicylateen_US
dc.subject.emtree5-nitroso-salicylateen_US
dc.subject.emtreeChromiumen_US
dc.subject.emtreeSalicylic aciden_US
dc.subject.emtreeSalicylic acid derivativeen_US
dc.subject.emtreeWateren_US
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