Hydrogen Peroxide Oxygenation of Alkanes Including Methane and Ethane Catalyzed by Iron Complexes in Acetonitrile
- 1 February 2004
- journal article
- research article
- Published by Wiley in Advanced Synthesis & Catalysis
- Vol. 346 (2-3) , 317-332
- https://doi.org/10.1002/adsc.200303147
Abstract
This paper describes an investigation of the alkane oxidation with hydrogen peroxide in acetonitrile catalyzed by iron(III) perchlorate (1), iron(III) chloride (2), iron(III) acetate (3) and a binuclear iron(III) complex with 1,4,7‐triazacyclononane (4). The corresponding alkyl hydroperoxides are the main products. Nevertheless in the kinetic study of cyclohexane oxidation, the concentrations of oxygenates (cyclohexanone and cyclohexanol) were measured after reduction of the reaction solution with triphenylphosphine (which converts the cyclohexyl hydroperoxide to the cyclohexanol). Methane and ethane can be also oxidized with TONs up to 30 and 70, respectively. Chloride anions added to the oxidation solution with 1 activate the perchlorate iron derivative in acetonitrile, whereas the water as additive inactivates 2 in the H2O2 decomposition process. Pyrazine‐2‐carboxylic acid (PCA) added to the reaction mixture decreases the oxidation rate if 1 or 2 are used as catalysts, whereas compounds 3 and 4 are active as catalysts only in the presence of small amount of PCA. The investigation of kinetics and selectivities of the oxidations demonstrated that the mechanisms of the reactions are different. Thus, in the oxidations catalyzed by the 1, 3+PCA and 4+PCA systems the main oxidizing species is hydroxyl radical, and the oxidation in the presence of 2 as a catalyst has been assumed to proceed (partially) with the formation of ferryl ion, (FeIVO)2+. In the oxidation catalyzed by the 4+PCA system (TONs attain 240) hydroxyl radicals were generated in the rate‐determining step of monomolecular decomposition of the iron diperoxo adduct containing one PCA molecule. A kinetic model of the process which satisfactorily describes the whole set of experimental data was suggested. The constants of supposed equilibriums and the rate constant for the decomposition of the iron diperoxo adduct with PCA were estimated.Keywords
This publication has 124 references indexed in Scilit:
- A Dramatic Push Effect on the Homolysis of FeIII(OOR) Intermediates To Form Non‐Heme FeIVO ComplexesAngewandte Chemie International Edition in English, 2003
- Epoxidation of Olefins by Hydroperoxo−Ferric Cytochrome P450Journal of the American Chemical Society, 2003
- Valence-tautomerism in high-valent iron and manganese porphyrinsJBIC Journal of Biological Inorganic Chemistry, 2001
- Hydroxylation of alkanes catalysed by a chiral μ-oxo diferric complex: a metal-based mechanismJournal of Molecular Catalysis A: Chemical, 2000
- Kinetics of hydrogen peroxide decomposition with complexed and ?free? iron catalystsInternational Journal of Chemical Kinetics, 1999
- Functional models for iron-bleomycinJournal of Molecular Catalysis A: Chemical, 1997
- Alkane oxidation catalyzed by μ-oxo bridged diferric complexes: an overall mechanismJournal of Molecular Catalysis A: Chemical, 1996
- Formation of alkyl peroxides in oxidation of alkanes by H2O2 catalyzed by transition metal complexesReaction Kinetics, Mechanisms and Catalysis, 1992
- Electronic and vibrational spectroscopic analysis of the (.mu.-oxo)bis(.mu.-carboxylato)diiron(III) core: a study of [Fe2O(O2CCH3)2(TACN)2]2+Inorganic Chemistry, 1985
- Initiation process in the system Fe3+ + H2O2International Journal of Chemical Kinetics, 1974