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Süss-Fink, Georg

Nom
Süss-Fink, Georg
Affiliation principale
Fonction
Professeur ordinaire
Email
georg.suess-fink@unine.ch
Identifiants
https://libra.unine.ch/handle/123456789/385

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  • Publication
    Métadonnées seulement
    Oxidation of 2-propanol and cyclohexane by the reagent "Hydrogen peroxide - Vanadate anion - Pyrazine-2-carboxylic acid": Kinetics and Mechanism
    (2007)
    Kozlov, Yuriy N
    ;
    Romakh, Vladimir B
    ;
    Kitaygorodskiy, Alex
    ;
    Buglyo, Peter
    ;
    Süss-Fink, Georg 
    ;
    Shul'pin, Georgiy B
    The vanadate anion in the presence of pyrazine-2-carboxylic acid (PCA equivalent to pcaH) efficiently catalyzes the oxidation of 2-propanol by hydrogen peroxide to give acetone. UV-vis spectroscopic monitoring of the reaction as well as the kinetics lead to the conclusion that the crucial step of the process is the monomolecular decomposition of a diperoxovanadium(V) complex containing the pca ligand to afford the peroxyl radical, HOO center dot and a V(IV) derivative. The rate-limiting step in the overall process may not be this (rapid) decomposition itself but (prior to this step) the slow hydrogen transfer from a coordinated H2O2 molecule to the oxygen atom of a pca ligand at the vanadium center: "(pca)(O)V center dot center dot center dot O2H2" -> "(pca)(HO-)V-OOH". The V(IV) derivative reacts with a new hydrogen peroxide molecule to generate the hydroxyl radical ("V-IV" + H2O2 -> "V-V" + HO- + HO center dot), active in the activation of isopropanol: HO center dot + Me2CH(OH) -> H2O + Me2C center dot(OH). The reaction with an alkane, RH, in acetonitrile proceeds analogously, and in this case the hydroxyl radical abstracts a hydrogen atom from the alkane: HO center dot + RH -> H2O + R-center dot. These conclusions are in a good agreement with the results obtained by Bell and co-workers (Khaliullin, R. Z.; Bell, A. T.; Head-Gordon, M. J. Phys. Chem. B 2005, 109, 17984-17992) who recently carried out a density functional theory study of the mechanism of radical generation in the reagent under discussion in acetonitrile.
  • Publication
    Métadonnées seulement
    Oxidations by the reagent ?O 2?H 2 O 2?vanadium derivative?pyrazine-2-carboxylic acid?. Part 12. Main features, kinetics and mechanism of alkane hydroperoxidation
    (2001)
    Shul'pin, Georgiy B
    ;
    Kozlov, Yuriy N
    ;
    Nizova, Galina V
    ;
    Süss-Fink, Georg 
    ;
    Stanislas, Sandrine
    ;
    Kitaygorodskiy, Alex
    ;
    Kulikova, Vera S
  • Publication
    Accès libre
    Oxidations by the reagent "O2–H2O2–vanadium derivative–pyrazine-2-carboxylic acid". Part 12.1 Main features, kinetics and mechanism of alkane hydroperoxidation
    (2001)
    Shulpin, Georgiy B.
    ;
    Kozlov, Yuriy N.
    ;
    Nizova, Galina V.
    ;
    Süss-Fink, Georg 
    ;
    Stanislas, Sandrine
    ;
    Kitaygorodskiy, Alex
    ;
    Kulikova, Vera S.
    Various combinations of vanadium derivatives (n-Bu4NVO3 is the best catalyst) with pyrazine-2-carboxylic acid (PCA) catalyse the oxidation of saturated hydrocarbons, RH, with hydrogen peroxide and air in acetonitrile solution to produce, at temperatures <40 °C, alkyl hydroperoxides, ROOH, as the main primary products. These compounds are easily reduced with triphenylphosphine to the corresponding alcohols, which can then be quantitatively determined by GLC. Certain aminoacids similar to PCA can play the role of co-catalyst; however the oxidation rates and final product yields are lower for picolinic and imidazole-4,5-dicarboxylic acids, while imidazole-4-carboxylic and pyrazole-3,5-dicarboxylic acids are almost inactive. The oxidation is induced by the attack of a hydroxyl radical on the alkane, RH, to produce alkyl radicals, R•. The latter further react rapidly with molecular atmospheric oxygen. The peroxyl radicals, ROO•, thus formed can be converted to alkyl hydroperoxides. We conclude on the basis of our kinetic investigation of the oxidation of cyclohexane that the rate-limiting step of the reaction is the monomolecular decomposition of the complex containing one coordinated PCA molecule: VV (PCA)(H2O2) → VIV (PCA) + HOO• + H+. The VIV species thus formed reacts further with a second H2O2 molecule to generate the hydroxyl radical according to the equation VIV (PCA) + H2O2→ VV (PCA) + HO• + HO–. The concentration of the active species in the course of the catalytic process has been estimated to be as low as [V(PCA)H2O2] ≈ 3.3 × 10–6 mol dm–3. The effective rate constant for the cyclohexane oxidation (d[ROOH]/dt = keff[H2O2]0[V]0) is keff = 0.44 dm3 mol–1 s–1 at 40 °C, the effective activation energy is 17 ± 2 kcal mol–1. It is assumed that the accelerating role of PCA is due to its facilitating the proton transfer between the oxo and hydroxy ligands of the vanadium complex on the one hand and molecules of hydrogen peroxide and water on the other hand. For example: (pca)(O=)V•••H2O2→ (pca)(HO–)V–OOH. Such a « robots arm mechanism » has analogies in enzyme catalysis.