Kinetics and mechanism of oxidation of apple pectin by CrVI in aqueous acid medium

BELLÚ, S. E.; GONZÁLEZ, J. C.; GARCÍA, S. I.; SIGNORELLA, S. R.; SALA, L. F.

JOURNAL OF PHYSICAL ORGANIC CHEMISTRY

John Wiley & Sons Ltd

Lugar: Chichester (UK); Año: 2008 vol. 21 p. 1059 - 1067

0894-3230

Selective oxidation of galacturonic acid residues of apple pectin by CrVI affords CO2/HCO2H, oxidized pectin and CrIII as final redox products. The reaction shows first order kinetics in [pectin], [CrVI] and [H+], at fixed ionic strength and temperature. Kinetic studies show that the redox reaction proceeds through a mechanism combining CrVI ® CrIV ® CrII and CrVI ® CrIV ® CrIII pathways. The mechanism is supported by the observation of free radicals, CrO22+ (the formation of which implies involvement of CrII and CrIV) and CrV (formed in monoelectronic redox processes) as reaction intermediates. The reduction of CrIV and CrV by pectin was independently studied and found to occur more than 103 times faster than pectin + CrVI reaction, in acid medium. At pH 3-5, apple pectin + CrVI redox reaction is slow, oxo-chromate(V)-pectin species stabilize and remain in solution during several hours. The present results show that these abundant and ubiquitous components of the cell walls of all land plants are able to reduce CrIV-VI or stabilize high-valent chromium depending on pH.