http://www.cnr.it/ontology/cnr/individuo/prodotto/ID283414
Hydrogen Production by Selective Dehydrogenation of HCOOH Catalyzed by Ru-biaryl Sulfonated Phosphines in Aqueous Solution (Articolo in rivista)
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- Label
- Hydrogen Production by Selective Dehydrogenation of HCOOH Catalyzed by Ru-biaryl Sulfonated Phosphines in Aqueous Solution (Articolo in rivista) (literal)
- Anno
- 2014-01-01T00:00:00+01:00 (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
- 10.1021/cs500655x (literal)
- Alternative label
Guerriero, Antonella; Bricout, Herve; Sordakis, Katerina; Peruzzini, Maurizio; Monflier, Eric; Hapiot, Frederic; Laurenczy, Gabor; Gonsalvi, Luca (2014)
Hydrogen Production by Selective Dehydrogenation of HCOOH Catalyzed by Ru-biaryl Sulfonated Phosphines in Aqueous Solution
in ACS catalysis; ACS, American chemical society, Washington, DC (Stati Uniti d'America)
(literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
- Guerriero, Antonella; Bricout, Herve; Sordakis, Katerina; Peruzzini, Maurizio; Monflier, Eric; Hapiot, Frederic; Laurenczy, Gabor; Gonsalvi, Luca (literal)
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- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroVolume
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- ISI Web of Science (WOS) (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
- Consiglio Nazionale delle Ricerche, Istituto di Chimica dei Composti Organometallici (ICCOM-CNR), via Madonna del Piano 10, 50019 Sesto Fiorentino, Firenze, Italy; Université Lille Nord de France, CNRS UMR 8181, Unité de Catalyse et de Chimie du Solid, UCCS U Artois, Faculté Jean Perrin, rue Jean Souvraz, SP18, F-62307, Lens Cédex, France; Institut des Science et Ingénierie Chimiques, École Polytechnique Fédérale de Lausanne (EPFL), CH-1015, Lausanne, Switzerland. (literal)
- Titolo
- Hydrogen Production by Selective Dehydrogenation of HCOOH Catalyzed by Ru-biaryl Sulfonated Phosphines in Aqueous Solution (literal)
- 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. (literal)
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