Abstract
The electrochemical oxidation of catechol has been studied in the presence of p-nitroaniline as a nucleophile in aqueous media at the surface of glassy carbon electrode, using cyclic voltammetry. The products of electrosynthesis have been purified and characterized by Fourier-transform infrared (FT-IR), 1H nuclear magnetic resonance (NMR), 13C NMR, and distortionless enhancement by polarization transfer (DEPT), and the mechanism of anodic oxidation was deduced from voltammetric and spectroscopic data.
References
Rich PR (1982) Faraday Discuss Chem Soc 148:54
Sutherland HS, Higgs KC, Taylor NJ, Rodrigo R (2001) Tetrahedron 57:309
Bringmam G, Tasler S (2001) Tetrahedron 57:331
Das MR, Conner HD, Leniart DS, Freed JH (1970) J Am Chem Soc 92:2258
Leary G, Porter G (1970) J Chem Soc (A) 2273
Patai S, Rappoport Z (1987) The chemistry of quinonoid compounds. Wiley, New York
Nematollahi D, Golabi SM (2000) J Electroanalysis 481:208
Kiani A, Raoof JB, Ojani R (2006) Bull Electrochem 22:275
Morrison RT, Boyd RN (1987) Organic chemistry, 5th edn. Allyn and Bacon, USA, p 1087
Kiani A, Raoof JB, Nematollahi D, Ojani R (2005) Electroanalysis 17:1755
Papouchado L, Petrie G, Adams RN (1972) J Electroanal Chem 38:389
Rayn MD, Yueh A, Wen-Yu C (1980) J Electrochem Soc 127:1489
Nematollahi D, Golabi SM (1998) Bull Electrochem 14:97
Nematollahi D, Goodarzi H (2001) J Electroanal Chem 510:108
Acknowledgements
Financial support of this work from the Research Council of Mazandaran University is gratefully acknowledged.
Author information
Authors and Affiliations
Corresponding author
Rights and permissions
About this article
Cite this article
Khaleghi, F., Khalilzadeh, M.A., Raoof, J.B. et al. Electrochemical oxidation of catechol in the presence of an aromatic amine in aqueous media. J Appl Electrochem 39, 1651–1654 (2009). https://doi.org/10.1007/s10800-009-9846-x
Received:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s10800-009-9846-x