Please use this identifier to cite or link to this item: http://hdl.handle.net/11452/25203
Title: Potentiometric and spectroscopic studies on aluminium(III) complexes of some catechol derivatives
Authors: Uludağ Üniversitesi/Fen-Edebiyat Fakültesi/Kimya Bölümü.
Türkel, Naciye
Berker, Melek
Özer, Ulviye
56630903300
9637276000
6601993613
Keywords: Pharmacology and pharmacy
Chemistry
Aluminium
Benzoic acid
Complex
Coordination compound
Acid Dissociation-constants
Oxovanadium(IV)
Complexes
Physiological conditions
Stability-constants
Biological-fluids
Metal-complexes
Manganese(II)
Equilibria
Iron(III)
Al(III)
Issue Date: Aug-2004
Publisher: Pharmaceutical Soc Japan
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.
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.
URI: https://doi.org/10.1248/cpb.52.929
https://www.jstage.jst.go.jp/article/cpb/52/8/52_8_929/_pdf/-char/en
http://hdl.handle.net/11452/25203
ISSN: 0009-2363
Appears in Collections:Scopus
Web of Science

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