Publication: Potentiometric and spectroscopic studies on aluminium(III) complexes of some catechol derivatives
dc.contributor.buuauthor | Türkel, Naciye | |
dc.contributor.buuauthor | Berker, Melek | |
dc.contributor.buuauthor | Özer, Ulviye | |
dc.contributor.department | Fen Edebiyat Fakültesi | |
dc.contributor.department | Kimya Bölümü | |
dc.contributor.scopusid | 56630903300 | |
dc.contributor.scopusid | 9637276000 | |
dc.contributor.scopusid | 6601993613 | |
dc.date.accessioned | 2022-03-21T07:05:28Z | |
dc.date.available | 2022-03-21T07:05:28Z | |
dc.date.issued | 2004-08 | |
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. | |
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. | |
dc.identifier.endpage | 934 | |
dc.identifier.issn | 0009-2363 | |
dc.identifier.issue | 8 | |
dc.identifier.pubmed | 15304983 | |
dc.identifier.scopus | 2-s2.0-16644401829 | |
dc.identifier.startpage | 929 | |
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.identifier.volume | 52 | |
dc.identifier.wos | 000223208200004 | |
dc.indexed.wos | SCIE | |
dc.language.iso | en | |
dc.publisher | Pharmaceutical Soc Japan | |
dc.relation.journal | Chemical and Pharmaceutical Bulletin | |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi | |
dc.rights | info:eu-repo/semantics/openAccess | |
dc.subject | Pharmacology and pharmacy | |
dc.subject | Chemistry | |
dc.subject | Aluminium | |
dc.subject | Benzoic acid | |
dc.subject | Complex | |
dc.subject | Coordination compound | |
dc.subject | Acid Dissociation-constants | |
dc.subject | Oxovanadium(IV) | |
dc.subject | Complexes | |
dc.subject | Physiological conditions | |
dc.subject | Stability-constants | |
dc.subject | Biological-fluids | |
dc.subject | Metal-complexes | |
dc.subject | Manganese(II) | |
dc.subject | Equilibria | |
dc.subject | Iron(III) | |
dc.subject | Al(III) | |
dc.subject.emtree | 2,3 dihydroxybenzoic acid | |
dc.subject.emtree | 3,4 dihydroxyphenylacetic acid | |
dc.subject.emtree | Aluminum 111 | |
dc.subject.emtree | Catechol derivative | |
dc.subject.emtree | Dihydrocaffeic acid | |
dc.subject.emtree | Ligand | |
dc.subject.emtree | Metal derivative | |
dc.subject.emtree | Protocatechuic acid | |
dc.subject.emtree | Proton | |
dc.subject.emtree | Salicylic acid | |
dc.subject.emtree | Unclassified drug | |
dc.subject.emtree | Aluminum derivative | |
dc.subject.emtree | Benzoic acid derivative | |
dc.subject.emtree | Chelating agent | |
dc.subject.emtree | Aqueous solution | |
dc.subject.emtree | Article | |
dc.subject.emtree | Chelation | |
dc.subject.emtree | Chemical analysis | |
dc.subject.emtree | Complex formation | |
dc.subject.emtree | Potentiometry | |
dc.subject.emtree | Proton transport | |
dc.subject.emtree | Spectroscopy | |
dc.subject.emtree | Titrimetry | |
dc.subject.emtree | Chemistry | |
dc.subject.emtree | Comparative study | |
dc.subject.emtree | Methodology | |
dc.subject.emtree | Potentiometry | |
dc.subject.emtree | Ultraviolet spectrophotometry | |
dc.subject.mesh | Aluminum compounds | |
dc.subject.mesh | Benzoates | |
dc.subject.mesh | Catechols | |
dc.subject.mesh | Chelating agents | |
dc.subject.mesh | Ligands | |
dc.subject.mesh | Potentiometry | |
dc.subject.mesh | Protons | |
dc.subject.mesh | Spectrophotometry, ultraviolet | |
dc.subject.scopus | Beryllium; Electrospray Ionization; Ligands | |
dc.subject.wos | Chemistry, medicinal | |
dc.subject.wos | Chemistry, multidisciplinary | |
dc.subject.wos | Pharmacology and pharmacy | |
dc.title | Potentiometric and spectroscopic studies on aluminium(III) complexes of some catechol derivatives | |
dc.type | Article | |
dc.wos.quartile | Q3 | |
dc.wos.quartile | Q2 (Chemistry, multidisciplinary) | |
dspace.entity.type | Publication | |
local.contributor.department | Fen Edebiyat Fakültesi/Kimya Bölümü | |
local.indexed.at | Scopus | |
local.indexed.at | WOS |