Mononuclear and Binuclear Wirelike Ruthenium(II) Complexes with Oligo-diethynyl-thiophene Bridged Back-to-Back Terpyridine Ligands: Synthesis and Electrochemical and Photophysical Properties (Articolo in rivista)

Type
Label
  • Mononuclear and Binuclear Wirelike Ruthenium(II) Complexes with Oligo-diethynyl-thiophene Bridged Back-to-Back Terpyridine Ligands: Synthesis and Electrochemical and Photophysical Properties (Articolo in rivista) (literal)
Anno
  • 2004-01-01T00:00:00+01:00 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
  • 10.1021/ic0493043 (literal)
Alternative label
  • A. Barbieri; B. Ventura; F. Barigelletti; A. De Nicola; M. Quesada; R. Ziessel (2004)
    Mononuclear and Binuclear Wirelike Ruthenium(II) Complexes with Oligo-diethynyl-thiophene Bridged Back-to-Back Terpyridine Ligands: Synthesis and Electrochemical and Photophysical Properties
    in Inorganic chemistry
    (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
  • A. Barbieri; B. Ventura; F. Barigelletti; A. De Nicola; M. Quesada; R. Ziessel (literal)
Pagina inizio
  • 7359 (literal)
Pagina fine
  • 7368 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroVolume
  • 43 (literal)
Rivista
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroFascicolo
  • 23 (literal)
Note
  • ISI Web of Science (WOS) (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
  • 1. CNR, ISOF, I-40129 Bologna, Italy 2. ULP, ECPM, F-67087 Strasbourg 02, France (literal)
Titolo
  • Mononuclear and Binuclear Wirelike Ruthenium(II) Complexes with Oligo-diethynyl-thiophene Bridged Back-to-Back Terpyridine Ligands: Synthesis and Electrochemical and Photophysical Properties (literal)
Abstract
  • The syntheses, structural features, electrochemical behavior, absorption spectra, and photophysical properties of five mononuclear complexes [(terpy)Ru(terpy-DEDBTn-terpy)](2+), RuTn, and five binuclear complexes [(terpy)Ru(terpy-DEDBTn-terpy)Ru(terpy)](4+), RuTnRu, are reported, where n varies from 1 to 5 so that the metal-metal distance is estimated to be 42 Angstrom for the largest binuclear complex, RuT5Ru (terpy is 2,2':6',2\"-terpyridine and DEDBT is 2,5-diethynyl-3,4-dibutylthiophene). The metal-centered oxidation potentials for the mononuclear and binuclear species are slightly more positive than for the reference [Ru(terpy)(2)](2+) complex, owing to the withdrawing nature of the back-to-back terpyridine ligands incorporating the repeat diethynyl-thiophene units. Comparison of the reduction potentials for the mononuclear and binuclear complexes reveals that the reduction steps are localized either at the terpy fragments of the T, ligands or at the terpy peripheral ligands. The spectroscopic results (absorption spectra at room temperature, luminescence spectra and lifetimes at room temperature and at 77 K) in acetonitrile solvent are consistent with the establishment of electronic delocalization within the oligomeric diethynyl-thiophene fragments (DEDBT,) of the T, ligands; however, the results also indicate that the terpy units of these ligands and the DEDBT, fragments are not strongly coupled. Both at room temperature and at 77 K, the 3 metal-to-ligand charge-transfer luminescence of RuTn and RuTnRu complexes is strongly depressed in the larger species with respect to what happens for n less than or equal to 2 (where the luminescence quantum yield is phi approximate to 10(-4)); this is discussed in terms of the possible intervention of triplet levels localized at the oligothiophene DEDBTn fragments. (literal)
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