Please use this identifier to cite or link to this item: http://hdl.handle.net/11452/25203
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dc.date.accessioned2022-03-21T07:05:28Z-
dc.date.available2022-03-21T07:05:28Z-
dc.date.issued2004-08-
dc.identifier.citationTürkel, N. vd. (2004). “Potentiometric and spectroscopic studies on aluminium(III) complexes of some catechol derivatives”. Chemical and Pharmaceutical Bulletin, 52(8), 929-934.en_US
dc.identifier.issn0009-2363-
dc.identifier.urihttps://doi.org/10.1248/cpb.52.929-
dc.identifier.urihttps://www.jstage.jst.go.jp/article/cpb/52/8/52_8_929/_pdf/-char/en-
dc.identifier.urihttp://hdl.handle.net/11452/25203-
dc.description.abstractThe interactions of aluminium(III) ion with the triprotic catechol derivatives (H3L), 2,3-dihydroxybenzoic acid (2,3-DHBA), 3,4-dihydroxyphenylacetic acid (3,4-DHPA), 3,4-dihydroxybenzoic acid (3,4-DHBA), and 3,4-dihydroxyhydrocinnamic acid (3,4-DHHCA) were investigated in aqueous solution at 25.0degreesC. The Calvin-Bjerrum titration method was adopted for the determination of formation constants of proton-ligand and aluminium(III)-ligand complexes. Potentiometric and spectroscopic results indicated that these catechol derivatives exhibit a true bidentate character. The chelation occurs via their catecholate sites, with the exception of 2,3-DHBA. In the case of 2,3-DHBA complexes, the dominant species are either the salicylate type (COO-, O-) or catecholate type (O-, O-) complex. The protonation constants of ligands and their formation constants of AI(III) complexes were also correlated. The order of decreasing stabilities of complexes is: 3,4-DHPA>3,4DHBA>3,4-DHHCA>2,3-DHBA.en_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.subjectAluminiumen_US
dc.subjectBenzoic aciden_US
dc.subjectComplexen_US
dc.subjectCoordination compounden_US
dc.subjectAcid Dissociation-constantsen_US
dc.subjectOxovanadium(IV)en_US
dc.subjectComplexesen_US
dc.subjectPhysiological conditionsen_US
dc.subjectStability-constantsen_US
dc.subjectBiological-fluidsen_US
dc.subjectMetal-complexesen_US
dc.subjectManganese(II)en_US
dc.subjectEquilibriaen_US
dc.subjectIron(III)en_US
dc.subjectAl(III)en_US
dc.subject.meshAluminum compoundsen_US
dc.subject.meshBenzoatesen_US
dc.subject.meshCatecholsen_US
dc.subject.meshChelating agentsen_US
dc.subject.meshLigandsen_US
dc.subject.meshPotentiometryen_US
dc.subject.meshProtonsen_US
dc.subject.meshSpectrophotometry, ultravioleten_US
dc.titlePotentiometric and spectroscopic studies on aluminium(III) complexes of some catechol derivativesen_US
dc.typeArticleen_US
dc.identifier.wos000223208200004tr_TR
dc.identifier.scopus2-s2.0-16644401829tr_TR
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergitr_TR
dc.contributor.departmentUludağ Üniversitesi/Fen-Edebiyat Fakültesi/Kimya Bölümü.tr_TR
dc.identifier.startpage929tr_TR
dc.identifier.endpage934tr_TR
dc.identifier.volume52tr_TR
dc.identifier.issue8tr_TR
dc.relation.journalChemical and Pharmaceutical Bulletinen_US
dc.contributor.buuauthorTürkel, Naciye-
dc.contributor.buuauthorBerker, Melek-
dc.contributor.buuauthorÖzer, Ulviye-
dc.identifier.pubmed15304983tr_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.scopusid56630903300tr_TR
dc.contributor.scopusid9637276000tr_TR
dc.contributor.scopusid6601993613tr_TR
dc.subject.scopusBeryllium; Electrospray Ionization; Ligandsen_US
dc.subject.emtree2,3 dihydroxybenzoic aciden_US
dc.subject.emtree3,4 dihydroxyphenylacetic aciden_US
dc.subject.emtreeAluminum 111en_US
dc.subject.emtreeCatechol derivativeen_US
dc.subject.emtreeDihydrocaffeic aciden_US
dc.subject.emtreeLiganden_US
dc.subject.emtreeMetal derivativeen_US
dc.subject.emtreeProtocatechuic aciden_US
dc.subject.emtreeProtonen_US
dc.subject.emtreeSalicylic aciden_US
dc.subject.emtreeUnclassified drugen_US
dc.subject.emtreeAluminum derivativeen_US
dc.subject.emtreeBenzoic acid derivativeen_US
dc.subject.emtreeChelating agenten_US
dc.subject.emtreeAqueous solutionen_US
dc.subject.emtreeArticleen_US
dc.subject.emtreeChelationen_US
dc.subject.emtreeChemical analysisen_US
dc.subject.emtreeComplex formationen_US
dc.subject.emtreePotentiometryen_US
dc.subject.emtreeProton transporten_US
dc.subject.emtreeSpectroscopyen_US
dc.subject.emtreeTitrimetryen_US
dc.subject.emtreeChemistryen_US
dc.subject.emtreeComparative studyen_US
dc.subject.emtreeMethodologyen_US
dc.subject.emtreePotentiometryen_US
dc.subject.emtreeUltraviolet spectrophotometryen_US
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