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Lebegue, E., Brousse, T., Gaubicher, J. & Cougnon, C. (2013) Spontaneous arylation of activated carbon from aminobenzene organic acids as source of diazonium ions in mild conditions. Electrochim. Acta, 88 680–687.
Added by: Laurent Cournède (2016-03-10 21:23:31) |
| Type de référence: Article DOI: 10.1016/j.electacta.2012.10.132 Numéro d'identification (ISBN etc.): 0013-4686 Clé BibTeX: Lebegue2013a Voir tous les détails bibliographiques  |
Catégories: ST2E Mots-clés: activated carbon, amines, Aminobenzene organic acid, anthranilic acids, aprotic diazotization, derivatives, Diazonium salts, electrochemical derivatization, electrochemistry, Electrode, metallic surfaces, nitro precursors, salts, Spontaneous grafting, triazenes Créateurs: Brousse, Cougnon, Gaubicher, Lebegue Collection: Electrochim. Acta |
Consultations : 13/1024
Indice de consultation : 1% Indice de popularité : 0.25% |
| Résumé |
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Activated carbon products modified with benzoic, benzenesulfonic and benzylphosphonic acid groups were prepared by spontaneous reduction of aryldiazonium ions in situ generated in water from the corresponding aminobenzene organic acids without addition of an external acid. Electrochemistry and NMR studies show that the advancement of the diazotization reaction depends both on the acidity and the electronic effect of the organic acid substituent, giving a mixture of diazonium, amine and triazene functionalities. Carbon products prepared by reaction of activated carbon Norit with 4-aminobenzenecarboxylic acid, 4-aminobenzenesulfonic acid and (4-aminobenzyl)phosphonic acid were analyzed by chemical elemental analysis and X-ray photoelectron spectroscopy experiments. Results show that this strategy is well suited for the chemical functionalization, giving a maximized grafting yield due to a chemical cooperation of amine and diazonium functionalities. (c) 2012 Elsevier Ltd. All rights reserved.
Added by: Laurent Cournède |