Please use this identifier to cite or link to this item: http://hdl.handle.net/11452/24072
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dc.date.accessioned2022-01-13T09:02:17Z-
dc.date.available2022-01-13T09:02:17Z-
dc.date.issued2005-03-
dc.identifier.citationTürkel, N. ve Özer, U. (2005). "Potentiometric investigations of some catechol derivatives of scandium". Russian Journal of Coordination Chemistry, 31(3), 213-217.en_US
dc.identifier.issn1070-3284-
dc.identifier.urihttps://doi.org/10.1007/s11173-005-0078-2-
dc.identifier.urihttps://link.springer.com/article/10.1007%2Fs11173-005-0078-2-
dc.identifier.urihttp://hdl.handle.net/11452/24072-
dc.description.abstractThe equilibrium reactions of scandium(III) with some triprotic catechol derivatives (H3L) were studied. The selected ligands that are 2,3-dihydroxybenzoic acid (2,3-DHBA), 3,4-dihydroxybenzoic acid (3,4-DHBA), 3.4-dihydroxyhydrocinnamic acid (3,4-DHHCA), and 3,4-dihydroxyphenylacetic acid (3,4-DHPA) were investigated in aqueous solution by means of potentiometry in 0.1 M ionic medium at 25 degrees C. The stability constants are reported for the ScL and ScL(H2L)(-) mononuclear complexes. 2,3-DHBA can bind to Sc3+ ion strongly and the salicylate mode (COO-, O-) is effective over the acidic pH range. But in higher pH range, 3,4-DHBA, 3,4-DHHCA, and 3,4-DHPA act more efficiently through catecholate groups (O-, O-).en_US
dc.language.isoenen_US
dc.publisherPleiades Publishingen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectChemistryen_US
dc.subjectAcid dissociation-constantsen_US
dc.subjectSalicylic-aciden_US
dc.subjectHydroxyaromatic ligandsen_US
dc.subjectDihydroxybenzoic acidsen_US
dc.subjectAqueous-solutionen_US
dc.subjectComplexesen_US
dc.subjectStabilitiesen_US
dc.subjectAluminumen_US
dc.subjectYttrium(III)en_US
dc.subjectEquilibriaen_US
dc.subjectCarboxylic acidsen_US
dc.subjectComplexationen_US
dc.subjectDerivativesen_US
dc.subjectMolecular structureen_US
dc.subjectPh effectsen_US
dc.subjectScandiumen_US
dc.subjectSolubilityen_US
dc.subjectCatechol derivativesen_US
dc.subjectIonic mediumen_US
dc.subjectPotentiometric investigationsen_US
dc.subjectStability constantsen_US
dc.subjectAlcoholsen_US
dc.titlePotentiometric investigations of some catechol derivatives of scandiumen_US
dc.typeArticleen_US
dc.identifier.wos000228191600013tr_TR
dc.identifier.scopus2-s2.0-17444397121tr_TR
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergitr_TR
dc.contributor.departmentUludağ Üniversitesi/Fen-Edebiyat Fakültesi/Kimya Bölümü.tr_TR
dc.identifier.startpage213tr_TR
dc.identifier.endpage217tr_TR
dc.identifier.volume31tr_TR
dc.identifier.issue3tr_TR
dc.relation.journalRussian Journal of Coordination Chemistryen_US
dc.contributor.buuauthorTürkel, Naciye-
dc.contributor.buuauthorÖzer, Ulviye-
dc.subject.wosChemistry, inorganic & nuclearen_US
dc.indexed.wosSCIEen_US
dc.indexed.scopusScopusen_US
dc.contributor.scopusid56630903300tr_TR
dc.contributor.scopusid6601993613tr_TR
dc.subject.scopusBeryllium; Electrospray Ionization; Complexationen_US
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