Synthesis and Near-infrared Luminescence of a Deuterated Conjugated Porphyrin Dimer for Probing the Mechanism of Non-radiative Deactivation (Articolo in rivista)

Type
Label
  • Synthesis and Near-infrared Luminescence of a Deuterated Conjugated Porphyrin Dimer for Probing the Mechanism of Non-radiative Deactivation (Articolo in rivista) (literal)
Anno
  • 2007-01-01T00:00:00+01:00 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
  • 10.1039/b700408g (literal)
Alternative label
  • Frampton M. J.; Accorsi G.; Armaroli N.; Rogers J. E.; Fleitz P. A.; McEwan K. J.; Anderson H. L. (2007)
    Synthesis and Near-infrared Luminescence of a Deuterated Conjugated Porphyrin Dimer for Probing the Mechanism of Non-radiative Deactivation
    in Organic & biomolecular chemistry
    (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
  • Frampton M. J.; Accorsi G.; Armaroli N.; Rogers J. E.; Fleitz P. A.; McEwan K. J.; Anderson H. L. (literal)
Pagina inizio
  • 1056 (literal)
Pagina fine
  • 1061 (literal)
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  • 5 (literal)
Rivista
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  • In: Organic & Biomolecular Chemistry, vol. 5 pp. 1056 - 1061. RSC- The Royal Society of Chemistry and Owner Societies, 2007. (literal)
Note
  • ISI Web of Science (WOS) (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
  • (a)Department of Chemistry, Chemistry Research Laboratory, Universityof Oxford, 12 Mansfield Road, Oxford, UK OX1 3TA. (b)Molecular Photoscience Group, Istituto per la Sintesi Organica e la Fotoreattivit`a, Consiglio Nazionale delle Ricerche, Via Gobetti 101, 40129, (c)Air ForceResearch Laboratory, AFRL/MLPJ, 3005 HobsonWay,Wright-Patterson Air Force Base, Dayton, Ohio, 45433-7702, USA (d)Defence Science and Technology Laboratory, St Andrews Road, Malvern, WR14 3PS, UK (literal)
Titolo
  • Synthesis and Near-infrared Luminescence of a Deuterated Conjugated Porphyrin Dimer for Probing the Mechanism of Non-radiative Deactivation (literal)
Abstract
  • beta,meso,beta-Fused porphyrin oligomers have many attractive photophysical features such as strong absorption in the near-IR at wavelengths greater than 1000 nm, and high two-photon cross sections. However their ultrafast S1-S0 deactivation (kd 1011 s-1) limits potential applications. We have synthesised a deuterated fused porphyrin dimer to test whether deuteration influences the rate of non-radiative deactivation. An efficient synthetic strategy was developed, starting with deuteration of dipyrromethane. Deuteration of the zinc porphyrin dimer does not affect its fluorescence quantum yield in CD2Cl2(fD/fH= 1.00 ± 0.05). This implies that the ultrafast non-radiative deactivation is not simply a consequence of the small S1-S0 energy gap. Comparison with other conjugated porphyrin oligomers confirms that the deactivation rate in the edge-fused oligomers is faster than would be expected from the energy gap law. This result indicates that it should be possible to create near-IR dyes with similar S1-S0 energy gaps to the beta,meso,beta-fused porphyrin oligomers but with slower rates of S1-S0 decay. (literal)
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