The selective dehydrogenation of aqueous solutions of HCOOH/HCOONa to H2 and CO2 gas mixtures has been investigated using RuCl3 x 3H2O as homogeneous catalyst precursor in the presence of different mono-aryl-biaryl or alkyl-biaryl phosphines and aryl diphosphines bearing sulfonated groups. All catalytic systems were used in water without any additives and proved to be active at 90 °C, giving high conversions and good TOF values. As an alternative Ru(II) metal precursor, the known dimer [Ru(eta6-C6H6)Cl2]2, was also tested as in situ catalyst with selected phosphines as well as an isolated Ru(II)-catalyst with one of them. By using High Pressure NMR (HPNMR) techniques, indications on the nature of the active species involved in the catalytic cycles were obtained.

Hydrogen Production by Selective Dehydrogenation of HCOOH Catalyzed by Ru-biaryl Sulfonated Phosphines in Aqueous Solution

Guerriero Antonella;Peruzzini Maurizio;Gonsalvi Luca
2014

Abstract

The selective dehydrogenation of aqueous solutions of HCOOH/HCOONa to H2 and CO2 gas mixtures has been investigated using RuCl3 x 3H2O as homogeneous catalyst precursor in the presence of different mono-aryl-biaryl or alkyl-biaryl phosphines and aryl diphosphines bearing sulfonated groups. All catalytic systems were used in water without any additives and proved to be active at 90 °C, giving high conversions and good TOF values. As an alternative Ru(II) metal precursor, the known dimer [Ru(eta6-C6H6)Cl2]2, was also tested as in situ catalyst with selected phosphines as well as an isolated Ru(II)-catalyst with one of them. By using High Pressure NMR (HPNMR) techniques, indications on the nature of the active species involved in the catalytic cycles were obtained.
2014
Istituto di Chimica dei Composti OrganoMetallici - ICCOM -
hydrogen
formic acid
ruthenium
water phase catalysis
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Descrizione: ACS Catal. 2014, 4, 3002-3012
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14243/256882
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