Efficient Greenish Blue Electrochemiluminescence from Fluorene and Spirobifluorene Derivatives (Articolo in rivista)

Type
Label
  • Efficient Greenish Blue Electrochemiluminescence from Fluorene and Spirobifluorene Derivatives (Articolo in rivista) (literal)
Anno
  • 2012-01-01T00:00:00+01:00 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
  • 10.1021/ja3054018 (literal)
Alternative label
  • Federico Polo, Fabio Rizzo, Manoel Veiga-Gutierrez, Luisa De Cola, Silvio Quici (2012)
    Efficient Greenish Blue Electrochemiluminescence from Fluorene and Spirobifluorene Derivatives
    in Journal of the American Chemical Society (Online); ACS, American chemical society, Washington, DC (Stati Uniti d'America)
    (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
  • Federico Polo, Fabio Rizzo, Manoel Veiga-Gutierrez, Luisa De Cola, Silvio Quici (literal)
Pagina inizio
  • 15402 (literal)
Pagina fine
  • 15409 (literal)
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  • http://pubs.acs.org/doi/abs/10.1021/ja3054018 (literal)
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  • 134 (literal)
Rivista
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  • 8 (literal)
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  • 37 (literal)
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  • Polo F.; Veiga-Gutierrez M.; De Cola L.: Physikalisches Institut, Westfälische Wilhelms-Universität, Heisenbergstrasse 11, D-48149 Münster, Germany (literal)
Titolo
  • Efficient Greenish Blue Electrochemiluminescence from Fluorene and Spirobifluorene Derivatives (literal)
Abstract
  • The spectroscopic and electrochemical behavior as well as electrogenerated chemiluminescence (ECL) of a series of donor-?-donor derivatives bearing triphenylamine groups as donor connected to a fluorene, 2,7-bis-(4-(N,Ndiphenylamino)phen-1-yl)-9,9?-dimethylfluorene (1), or spirobifluorene core, 2,7-bis-(4-(N,N-diphenylamino)phen-1-yl)-9,9?-spirobifluorene (2) and 2,2?,7,7?-tetrakis(4-(N,Ndiphenylamino)phen-1-yl)-9,9?-spirobifluorene (3), were investigated. Besides a high photoluminescence (PL) quantum yield in solution (between 81 and 87%), an efficient radical ions annihilation process induces intense greenish blue ECL emission that could be seen with the naked eye. Only the tetrasubstituted spirobifluorene derivative (compound 3) shows weak ECL obtained by a direct annihilation mechanism. Because the energy of the annihilation reaction is higher than the energy required to form the singlet excited state, the S-route could be considered the pathway followed by the ECL process in these molecules. The ECL emissions recorded by direct ion-ion annihilation show two bands compared to the single structureless PL band. The ECL spectra obtained by a coreactant approach using benzoylperoxide as a coreagent show no differences relative to that produced by annihilation, except for an increasing of ECL intensity for all compounds. (literal)
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