Complex formation between transition metal ions and salicylglycine, a metabolite of aspirin
GONZALEZ, E B and DAEID, N N and NOLAN, K B (1994) Complex formation between transition metal ions and salicylglycine, a metabolite of aspirin. Polyhedron, 13 (10). pp. 1495-1499. ISSN 0277-5387
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Ionization constants and complex formation constants of salicylglycine (1) in aqueous solution at 25-degrees-C and ionic strength 0.2 mol dm-3 KCl have been determined. The pK(a) values for the ligand are 3.44(1) and 8.24(4) and H-1 NMR studies show that there is no further ionization at higher pH as was previously suggested. In the case of copper(II) there is no evidence for complex formation below pH 4 and the main species in solution at pH>5 according to pH-metric and UV-vis spectrophotometric evidence in MLH-1 in which the ligand is bonded to the metal through the phenolate and carboxylate oxygen atoms and the deprotonated peptide nitrogen. The species ML also exists albeit in low concentrations. At pH>10 the formation of MLH-2 resulting from ionization of an equatorial aquo ligand is observed. In the case of nickel(II) and zinc(II) no complex formation occurs below pH 6 but above this pH the species ML and MLH-1, the latter involving deprotonation of an aquo ligand, are observed although at pH > ca 8 in the case of nickel(II) and pH > approximately 7.5 in the case of zinc(II) precipitation occurs.
Item type: Article ID code: 33466 Dates: DateEventMay 1994PublishedKeywords: copper, nickel, peptides, aspirin, Physical and theoretical chemistry, Electronic computers. Computer science, Materials Chemistry, Physical and Theoretical Chemistry, Inorganic Chemistry Subjects: Science > Chemistry > Physical and theoretical chemistry
Science > Mathematics > Electronic computers. Computer scienceDepartment: Faculty of Science > Pure and Applied Chemistry
Faculty of Science > Computer and Information SciencesDepositing user: Pure Administrator Date deposited: 17 Oct 2011 09:44 Last modified: 20 Jan 2021 19:33 URI: https://strathprints.strath.ac.uk/id/eprint/33466