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DC Field | Value | Language |
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dc.date.accessioned | 2022-03-21T07:05:28Z | - |
dc.date.available | 2022-03-21T07:05:28Z | - |
dc.date.issued | 2004-08 | - |
dc.identifier.citation | Türkel, 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.issn | 0009-2363 | - |
dc.identifier.uri | https://doi.org/10.1248/cpb.52.929 | - |
dc.identifier.uri | https://www.jstage.jst.go.jp/article/cpb/52/8/52_8_929/_pdf/-char/en | - |
dc.identifier.uri | http://hdl.handle.net/11452/25203 | - |
dc.description.abstract | The 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.iso | en | en_US |
dc.publisher | Pharmaceutical Soc Japan | en_US |
dc.rights | info:eu-repo/semantics/openAccess | en_US |
dc.rights | Atıf Gayri Ticari Türetilemez 4.0 Uluslararası | tr_TR |
dc.rights.uri | http://creativecommons.org/licenses/by-nc-nd/4.0/ | * |
dc.subject | Pharmacology and pharmacy | en_US |
dc.subject | Chemistry | en_US |
dc.subject | Aluminium | en_US |
dc.subject | Benzoic acid | en_US |
dc.subject | Complex | en_US |
dc.subject | Coordination compound | en_US |
dc.subject | Acid Dissociation-constants | en_US |
dc.subject | Oxovanadium(IV) | en_US |
dc.subject | Complexes | en_US |
dc.subject | Physiological conditions | en_US |
dc.subject | Stability-constants | en_US |
dc.subject | Biological-fluids | en_US |
dc.subject | Metal-complexes | en_US |
dc.subject | Manganese(II) | en_US |
dc.subject | Equilibria | en_US |
dc.subject | Iron(III) | en_US |
dc.subject | Al(III) | en_US |
dc.subject.mesh | Aluminum compounds | en_US |
dc.subject.mesh | Benzoates | en_US |
dc.subject.mesh | Catechols | en_US |
dc.subject.mesh | Chelating agents | en_US |
dc.subject.mesh | Ligands | en_US |
dc.subject.mesh | Potentiometry | en_US |
dc.subject.mesh | Protons | en_US |
dc.subject.mesh | Spectrophotometry, ultraviolet | en_US |
dc.title | Potentiometric and spectroscopic studies on aluminium(III) complexes of some catechol derivatives | en_US |
dc.type | Article | en_US |
dc.identifier.wos | 000223208200004 | tr_TR |
dc.identifier.scopus | 2-s2.0-16644401829 | tr_TR |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi | tr_TR |
dc.contributor.department | Uludağ Üniversitesi/Fen-Edebiyat Fakültesi/Kimya Bölümü. | tr_TR |
dc.identifier.startpage | 929 | tr_TR |
dc.identifier.endpage | 934 | tr_TR |
dc.identifier.volume | 52 | tr_TR |
dc.identifier.issue | 8 | tr_TR |
dc.relation.journal | Chemical and Pharmaceutical Bulletin | en_US |
dc.contributor.buuauthor | Türkel, Naciye | - |
dc.contributor.buuauthor | Berker, Melek | - |
dc.contributor.buuauthor | Özer, Ulviye | - |
dc.identifier.pubmed | 15304983 | tr_TR |
dc.subject.wos | Chemistry, medicinal | en_US |
dc.subject.wos | Chemistry, multidisciplinary | en_US |
dc.subject.wos | Pharmacology and pharmacy | en_US |
dc.indexed.wos | SCIE | en_US |
dc.indexed.scopus | Scopus | en_US |
dc.indexed.pubmed | Pubmed | en_US |
dc.wos.quartile | Q3 | en_US |
dc.wos.quartile | Q2 (Chemistry, multidisciplinary) | en_US |
dc.contributor.scopusid | 56630903300 | tr_TR |
dc.contributor.scopusid | 9637276000 | tr_TR |
dc.contributor.scopusid | 6601993613 | tr_TR |
dc.subject.scopus | Beryllium; Electrospray Ionization; Ligands | en_US |
dc.subject.emtree | 2,3 dihydroxybenzoic acid | en_US |
dc.subject.emtree | 3,4 dihydroxyphenylacetic acid | en_US |
dc.subject.emtree | Aluminum 111 | en_US |
dc.subject.emtree | Catechol derivative | en_US |
dc.subject.emtree | Dihydrocaffeic acid | en_US |
dc.subject.emtree | Ligand | en_US |
dc.subject.emtree | Metal derivative | en_US |
dc.subject.emtree | Protocatechuic acid | en_US |
dc.subject.emtree | Proton | en_US |
dc.subject.emtree | Salicylic acid | en_US |
dc.subject.emtree | Unclassified drug | en_US |
dc.subject.emtree | Aluminum derivative | en_US |
dc.subject.emtree | Benzoic acid derivative | en_US |
dc.subject.emtree | Chelating agent | en_US |
dc.subject.emtree | Aqueous solution | en_US |
dc.subject.emtree | Article | en_US |
dc.subject.emtree | Chelation | en_US |
dc.subject.emtree | Chemical analysis | en_US |
dc.subject.emtree | Complex formation | en_US |
dc.subject.emtree | Potentiometry | en_US |
dc.subject.emtree | Proton transport | en_US |
dc.subject.emtree | Spectroscopy | en_US |
dc.subject.emtree | Titrimetry | en_US |
dc.subject.emtree | Chemistry | en_US |
dc.subject.emtree | Comparative study | en_US |
dc.subject.emtree | Methodology | en_US |
dc.subject.emtree | Potentiometry | en_US |
dc.subject.emtree | Ultraviolet spectrophotometry | en_US |
Appears in Collections: | Scopus Web of Science |
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