Voici les éléments 1 - 3 sur 3
  • Publication
    Accès libre
    Ruthenium Nanoparticles Intercalated in Hectorite: A Reusable Hydrogenation Catalyst for Benzene and Toluene
    (2007) ;
    Mollwitz, Birgit
    ;
    ;
    Dadras, Massoud
    ;
    Laurenczy, Gabor
    ;
    Meister, Annette
    ;
    Meister, Götz
    The cationic organometallic aqua complexes formed by hydrolysis of [(C6H6)RuCl2]2 in water, mainly [(C6H6)Ru(H2O)3]2+, intercalate into sodium hectorite by ion exchange, replacing the sodium cations between the anionic silicate layers. The yellow hectorite thus obtained reacts in ethanol with molecular hydrogen (50 bar, 100°C) with decomposition of the organometallic aqua complexes to give a black material, in which ruthenium(0) nanoparticles (9–18 nm) are intercalated between the anionic silicate layers, the charges of which being balanced by hydronium cations. The black ruthenium-modified hectorite efficiently catalyses the hydrogenation of benzene and toluene in ethanol (50 bar H2, 50°C), the turnover frequencies attaining 7000 catalytic cycles per hour.
  • Publication
    Métadonnées seulement
    Mechanistic
    (2002)
    Laurenczy, Gábor
    ;
    Faure, Matthieu
    ;
    Vieille-Petit, Ludovic
    ;
    ;
    Ward, Thomas R
    In situ high-pressure NMR spectroscopy of the hydrogenation of benzene to give cyclohexane, catalysed by the cluster cation [(eta(6)-C6H6) (eta(6)-C6Me6)(2)Ru-3(mu(3)-O)(mu(2)-OH)(mu(2)-H)(2)](+) 2, supports a mechanism involving a supramolecular host-guest complex of the substrate molecule in the hydrophobic pocket of the intact cluster molecule.
  • Publication
    Accès libre
    Mechanistic in situ High-Pressure NMR Studies of Benzene Hydrogenation by Supramolecular Cluster Catalysis with [(η6-C6H6)(η6-C6Me6)2Ru33-O)(μ2-OH)(μ2-H)2][BF4]
    (2002)
    Laurenczy, Gabor
    ;
    Faure, Matthieu
    ;
    Vieille-Petit, Ludovic
    ;
    ;
    Ward, Thomas R.
    In situ high-pressure NMR spectroscopy of the hydrogenation of benzene to give cyclohexane, catalysed by the cluster cation [(η6-C6H6)(η6-C6Me6)2Ru33-O)(μ2-OH)(μ2-H)2]+2, supports a mechanism involving a supramolecular host-guest complex of the substrate molecule in the hydrophobic pocket of the intact cluster molecule.