Complex formation between oxovanadium(IV) and a series of aliphatic mercaptocarboxylic acids (mercaptoacetic, 2- and 3-mercaptopropionic, 2-mercaptosuccinic, and meso-2,3-dimercaptosuccinic) was studied in aqueous solution by potentiometric and spectroscopic (EPR and electronic absorption) techniques. A comparison with the complexes of the corresponding hydroxycarboxylic acid analogues was also made. The most interesting finding is that VO2+ has a similar affinity to the rather soft thiolate-S donors as to the hard alcoholate-O donors, if these donors are in chelatable position with a hard carboxylate group. The bidentate mercaptocarboxylates form (CO2-, S-)-co-ordinated mono and bis complexes, while bis complex formation is rather hindered with the tridentate 2-mercaptosuccinic acid. Due to the high denticity of the ligand, 2,3-dimercaptosuccinic acid readily forms oligomeric species via the co-ordination of all potential donor groups.

Oxovanadium(IV) complexes of mercaptocarboxylic acids.

Daniele Sanna
1993

Abstract

Complex formation between oxovanadium(IV) and a series of aliphatic mercaptocarboxylic acids (mercaptoacetic, 2- and 3-mercaptopropionic, 2-mercaptosuccinic, and meso-2,3-dimercaptosuccinic) was studied in aqueous solution by potentiometric and spectroscopic (EPR and electronic absorption) techniques. A comparison with the complexes of the corresponding hydroxycarboxylic acid analogues was also made. The most interesting finding is that VO2+ has a similar affinity to the rather soft thiolate-S donors as to the hard alcoholate-O donors, if these donors are in chelatable position with a hard carboxylate group. The bidentate mercaptocarboxylates form (CO2-, S-)-co-ordinated mono and bis complexes, while bis complex formation is rather hindered with the tridentate 2-mercaptosuccinic acid. Due to the high denticity of the ligand, 2,3-dimercaptosuccinic acid readily forms oligomeric species via the co-ordination of all potential donor groups.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14243/126363
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