Logo du site
  • English
  • Français
  • Se connecter
Logo du site
  • English
  • Français
  • Se connecter
  1. Accueil
  2. Université de Neuchâtel
  3. Publications
  4. The kinetics and mechanism of oxidation of isopropanol with the hydrogen peroxide-vanadate ion-pyrazine-2-carboxylic acid system
 
  • Details
Options
Vignette d'image

The kinetics and mechanism of oxidation of isopropanol with the hydrogen peroxide-vanadate ion-pyrazine-2-carboxylic acid system

Auteur(s)
Romakh, Vladimir B
Kozlov, Yuriy N
Süss-Fink, Georg 
Institut de chimie 
Shul'pin, Georgiy B
Date de parution
2007
In
Russian Journal of Physical Chemistry A
Vol.
8
No
81
De la page
1221
A la page
1229
Mots-clés
  • O-2-H2O2-VANADIUM DER...

  • H2O2-VANADIUM

  • COMPLEX-PYRAZINE-2-CA...

  • COMPLEX PYRAZINE-2-CA...

  • AEROBIC OXIDATION

  • VANADIUM COMPLEX

  • LOWER ALKANES

  • REAGENT

  • ACETONITRILE

  • OXYGENATION

  • METHANE

Résumé
The vanadate anion in the presence of pyrazine-2-carboxylic acid (PCA) was found to effectively catalyze the oxidation of isopropanol to acetone with hydrogen peroxide. The electronic spectra of solutions and the kinetics of oxidation were studied. The conclusion was drawn that the rate-determining stage of the reaction was the decomposition of the vanadium(V) diperoxo complex with PCA, and the particle that induced the oxidation of isopropanol was the hydroxyl radical. Supposedly, the HO center dot radical detached a hydrogen atom from isopropanol, and the Me2C center dot(OH) radical formed reacted with HOO center dot to produce acetone and hydrogen peroxide. The electronic spectra of solutions in isopropanol and acetonitrile and the dependences of the initial rates of isopropanol oxidation without a solvent and cyclohexane oxidation in acetonitrile on the initial concentration of hydrogen peroxide were compared. The conclusion was drawn that hydroxyl radicals appeared in the oxidation of alkanes in acetonitrile in the decomposition of the vanadium diperoxo complex rather than the monoperoxo derivative, as was suggested by us earlier.
URI
https://libra.unine.ch/handle/123456789/13406
Type de publication
Resource Types::text::journal::journal article
google-scholar
Présentation du portailGuide d'utilisationStratégie Open AccessDirective Open Access La recherche à l'UniNE Open Access ORCID

Adresse:
UniNE, Service information scientifique & bibliothèques
Rue Emile-Argand 11
2000 Neuchâtel

Construit avec Logiciel DSpace-CRIS Maintenu et optimiser par 4Sciences

  • Paramètres des témoins de connexion
  • Politique de protection de la vie privée
  • Licence de l'utilisateur final