[article]
Titre : |
Reaction kinetics and mechanism of copper(II) catalyzed oxidative deamination and decarboxylation of ornithine by peroxomonosulfate |
Type de document : |
texte imprimé |
Auteurs : |
Paramasivam Suresh Kumar, Auteur ; Radhakrishnan Mohan Raj, Auteur ; Srinivasalu Kutti Rani, Auteur |
Année de publication : |
2012 |
Article en page(s) : |
pp. 6310-6319 |
Note générale : |
Industrial chemistry |
Langues : |
Anglais (eng) |
Mots-clés : |
Oxidation Catalytic reaction Kinetics |
Résumé : |
Copper(II) catalyzed and uncatalyzed oxidation of ornithine by peroxomonosulfate (PMS) was studied in acetic acid–sodium acetate buffered medium (pH 3.6–5.2). The catalyzed reaction was 2.6 times faster than the uncatalyzed reaction. The catalytic constant kc obtained in this study was 0.15 mol–1 dm3 s–1. A negative value of entropy of activation obtained in this reaction revealed that the transition state was more rigid than the reactants. ESR spectral data ruled out the participation of free radical intermediate. Cyclic voltammetric and absorption studies confirmed the formation of copper–ornithine–PMS complex. HPLC analysis revealed that the product formed in this reaction was 4-aminobutanal, which was confirmed by NMR spectra. |
ISSN : |
0888-5885 |
En ligne : |
http://cat.inist.fr/?aModele=afficheN&cpsidt=25867282 |
in Industrial & engineering chemistry research > Vol. 51 N° 18 (Mai 2012) . - pp. 6310-6319
[article] Reaction kinetics and mechanism of copper(II) catalyzed oxidative deamination and decarboxylation of ornithine by peroxomonosulfate [texte imprimé] / Paramasivam Suresh Kumar, Auteur ; Radhakrishnan Mohan Raj, Auteur ; Srinivasalu Kutti Rani, Auteur . - 2012 . - pp. 6310-6319. Industrial chemistry Langues : Anglais ( eng) in Industrial & engineering chemistry research > Vol. 51 N° 18 (Mai 2012) . - pp. 6310-6319
Mots-clés : |
Oxidation Catalytic reaction Kinetics |
Résumé : |
Copper(II) catalyzed and uncatalyzed oxidation of ornithine by peroxomonosulfate (PMS) was studied in acetic acid–sodium acetate buffered medium (pH 3.6–5.2). The catalyzed reaction was 2.6 times faster than the uncatalyzed reaction. The catalytic constant kc obtained in this study was 0.15 mol–1 dm3 s–1. A negative value of entropy of activation obtained in this reaction revealed that the transition state was more rigid than the reactants. ESR spectral data ruled out the participation of free radical intermediate. Cyclic voltammetric and absorption studies confirmed the formation of copper–ornithine–PMS complex. HPLC analysis revealed that the product formed in this reaction was 4-aminobutanal, which was confirmed by NMR spectra. |
ISSN : |
0888-5885 |
En ligne : |
http://cat.inist.fr/?aModele=afficheN&cpsidt=25867282 |
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