Complex formation between transition metal ions and salicylglycine, a metabolite of aspirin

E B GONZALEZ, N N DAEID, K B NOLAN

Research output: Contribution to journalArticle

22 Citations (Scopus)

Abstract

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.

LanguageEnglish
Pages1495-1499
Number of pages5
JournalPolyhedron
Volume13
Issue number10
DOIs
Publication statusPublished - May 1994

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metabolites
Metabolites
Aspirin
Transition metals
Metal ions
metal ions
transition metals
Ligands
Ionization
Nickel
Zinc
Deprotonation
ligands
Ionic strength
Peptides
Copper
ionization
Nitrogen
Metals
Nuclear magnetic resonance

Keywords

  • copper
  • nickel
  • peptides
  • aspirin

Cite this

GONZALEZ, E B ; DAEID, N N ; NOLAN, K B . / Complex formation between transition metal ions and salicylglycine, a metabolite of aspirin. In: Polyhedron. 1994 ; Vol. 13, No. 10. pp. 1495-1499.
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abstract = "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.",
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Complex formation between transition metal ions and salicylglycine, a metabolite of aspirin. / GONZALEZ, E B ; DAEID, N N ; NOLAN, K B .

In: Polyhedron, Vol. 13, No. 10, 05.1994, p. 1495-1499.

Research output: Contribution to journalArticle

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AU - GONZALEZ, E B

AU - DAEID, N N

AU - NOLAN, K B

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N2 - 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.

AB - 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.

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