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Alkane oxygenation with H2O2 catalysed by FeCl3 and 2,2 '-bipyridine
Auteur(s)
Shul'pin, Georgiy B
Golfeto, Camilla C
Shul'pina, Lidia S
Mandelli, Dalma
Date de parution
2005
In
Tetrahedron Letters
Vol.
27
No
46
De la page
4563
A la page
4567
Mots-clés
- alkanes
- alkyl hydroperoxides
- biomimetics
- homogeneous catalysis
- hydrogen peroxide
- hydroperoxidation
- iron complexes
- oxygenation
- COMPLEX-CARBOXYLIC-ACID
- O-2-H2O2-VANADIUM
- DERIVATIVE-PYRAZINE-2-CARBOXYLIC ACID
- DINUCLEAR MANGANESE(IV) COMPLEX
- HYDROGEN-PEROXIDE
- IRON COMPLEXES
- HYDROCARBON OXIDATIONS
- DIFERRIC
- COMPLEXES
- ALKYL PEROXIDES
- METAL-COMPLEXES
- HYDROXYLATION
alkanes
alkyl hydroperoxides
biomimetics
homogeneous catalysis...
hydrogen peroxide
hydroperoxidation
iron complexes
oxygenation
COMPLEX-CARBOXYLIC-AC...
O-2-H2O2-VANADIUM
DERIVATIVE-PYRAZINE-2...
DINUCLEAR MANGANESE(I...
HYDROGEN-PEROXIDE
IRON COMPLEXES
HYDROCARBON OXIDATION...
DIFERRIC
COMPLEXES
ALKYL PEROXIDES
METAL-COMPLEXES
HYDROXYLATION
Résumé
The H2O2-FeCl3-bipy system in acetonitrile efficiently oxidises alkanes predominantly to alkyl hydroperoxides. Turnover numbers attain 400 after 1 h at 60 degrees C. It has been assumed that bipy facilitates proton abstraction from a H2O2 molecule coordinated to the iron ion (these reactions are stages in the catalytic cycle generating hydroxyl radicals from the hydrogen peroxide). Hydroxyl radicals then attack alkane molecules finally yielding the alkyl hydroperoxide. (c) 2005 Elsevier Ltd. All rights reserved.
Identifiants
Type de publication
journal article