Electrooxidation of ruthenium cyclopentadienyl PTA complexes in DMF: ESI-MS, cyclic voltammetry and on-line electrochemistry/ESI-MS s (Articolo in rivista)

Type
Label
  • Electrooxidation of ruthenium cyclopentadienyl PTA complexes in DMF: ESI-MS, cyclic voltammetry and on-line electrochemistry/ESI-MS s (Articolo in rivista) (literal)
Anno
  • 2007-01-01T00:00:00+01:00 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
  • 10.1149/1.2374938 (literal)
Alternative label
  • Gutkin, Vitaly; Gun, Jenny; Prikhodchenko, Petr V.; Lev, Ovadia; Gonsalvi, Luca; Peruzzini, Maurizio; Romerosa, Antonio; Campos-Malpartida, Tatiana; Lidrissi, Chaker (2007)
    Electrooxidation of ruthenium cyclopentadienyl PTA complexes in DMF: ESI-MS, cyclic voltammetry and on-line electrochemistry/ESI-MS s
    in Journal of the Electrochemical Society; Electrochemical Society, Pennington [NJ] (Stati Uniti d'America)
    (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
  • Gutkin, Vitaly; Gun, Jenny; Prikhodchenko, Petr V.; Lev, Ovadia; Gonsalvi, Luca; Peruzzini, Maurizio; Romerosa, Antonio; Campos-Malpartida, Tatiana; Lidrissi, Chaker (literal)
Pagina inizio
  • F7 (literal)
Pagina fine
  • F15 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroVolume
  • 154 (literal)
Rivista
Note
  • ISI Web of Science (WOS) (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
  • Laboratory of Environmental Chemistry, The Casali Institute, The Chemistry Institute, The Hebrew University of Jerusalem, Jerusalem 91904, Israel; Istituto di Chimica dei Composti Organo Metallici, Consiglio Nazionale delle Ricerche, 50019 Sesto Fiorentino, Italy; Area de Quimica Inorganica, Facultad de Ciencias Experimentales, Universidad de Almeria 04120, Almeria, Spain (literal)
Titolo
  • Electrooxidation of ruthenium cyclopentadienyl PTA complexes in DMF: ESI-MS, cyclic voltammetry and on-line electrochemistry/ESI-MS s (literal)
Abstract
  • Halogen complexes of ruthenium cyclopentadienyl ?CpRu?PTA?2X?; ?CpRu?PTA??PPh3?X?; ?CpRu?PPh3?2Cl?, and ?CpRu?mPTA??PPh3?X?+ ?Cp = C5H5; PTA = 1,3,5-triaza-7-phosphaadamantane; mPTA+ = ?1-methyl-1,3,5-triaza-7- phosphaadamantane?+; X = Cl-, I-? were investigated by electrospray mass spectrometry ?ESI-MS?, in flow-cell cyclic voltammetry, by microelectrodes, and by combined online electrochemistry and electrospray mass spectrometry ?EC/ESI-MS? in dimethyl formamide solution. Coordination changes and the structures of the initial compounds and the products of the electrooxidation of the Ru?II? complexes were traced by in situ EC/MSn experiments which revealed their fragmentation pathways. ESI-MS collision-induced dissociation fragmentations of the initial reactants and the oxidation products were explained by soft acid-hard base considerations taking into account the different nature of Ru?II?--Ru?IV? centers. The electrochemical studies show that it is possible to tune the formal potentials for the oxidation of ?CpRuL2X? complexes by over 300 mV by proper selection of the ligands. The increase of the redox potential by the different ligands follows the order PTA ? PPh3 ? mPTA+. We demonstrate a similarity between the propensity of the ligand to fragment out in the gas phase and its relationship to the formal potential of the complex. (literal)
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