Photophysical and Electrochemical Properties of Thiophene-Based 2-Arylpyridines (Articolo in rivista)

Type
Label
  • Photophysical and Electrochemical Properties of Thiophene-Based 2-Arylpyridines (Articolo in rivista) (literal)
Anno
  • 2011-01-01T00:00:00+01:00 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
  • 10.1002/ejoc.201100651 (literal)
Alternative label
  • Carmine Coluccini, Norberto Manfredi, Erika Herrera Calderon, Matteo M. Salamone, Riccardo Ruffo, Dominique Roberto, Maria Grazia Lobello, Filippo De Angelis, Alessandro Abbotto (2011)
    Photophysical and Electrochemical Properties of Thiophene-Based 2-Arylpyridines
    in European journal of organic chemistry (Online)
    (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
  • Carmine Coluccini, Norberto Manfredi, Erika Herrera Calderon, Matteo M. Salamone, Riccardo Ruffo, Dominique Roberto, Maria Grazia Lobello, Filippo De Angelis, Alessandro Abbotto (literal)
Pagina inizio
  • 5587 (literal)
Pagina fine
  • 5598 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#url
  • http://onlinelibrary.wiley.com/doi/10.1002/ejoc.201100651/abstract (literal)
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  • 2011 (literal)
Rivista
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  • 12 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroFascicolo
  • 28 (literal)
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  • Carmine Coluccini, Norberto Manfredi, Erika Herrera Calderon, Matteo M. Salamone, Riccardo Ruffo, Alessandro Abbotto: Department of Materials Science and Milano-Bicocca Solar Energy Research Center - MIB-Solar, University of MilanoBicocca, Via Cozzi 53, 20125 Milano, Italy Fax: +39-02-6448-5400 E-mail: alessandro.abbotto@unimib.it Dominique Roberto: Dipartimento di Chimica Inorganica, Metallorganica e Analitica, University of Milano, Via Venezian 21, 20133 Milano, Italy Maria Grazia Lobello, Filippo De Angelis: Istituto CNR di Scienze e Tecnologie Molecolari (ISTM-CNR), c/o Dipartimento di Chimica, Università di Perugia, Via Elce di Sotto 8, 06123 Perugia, Italy (literal)
Titolo
  • Photophysical and Electrochemical Properties of Thiophene-Based 2-Arylpyridines (literal)
Abstract
  • Two families of thiophene-based 2-arylpyridines, in which aryl is phenyl and 2,4-difluorophenyl, have been developed. The pyridine ring of the new compounds is substituted at the 4-position with ?-conjugated electron-rich and electron-poor thiophene-based fragments to tune the optical and energetic properties. The high-yielding synthetic access, which consists of two sequential Suzuki coupling reactions, the first of which is completely regioselective, is of wide applicability and allows access to a large variety of derivatives. The absorption/emission and redox features, as well as the HOMO and LUMO energy levels, have been investigated; the results show that the optical and electronic properties can be tuned over a broad range. The diversity of the characteristics may be effectively exploited by using the thiophene-substituted 2-arylpyridines as ligands in cyclometalated sensitizers for dye-sensitized solar cells and other optoelectronic applications. (literal)
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