4.7 Article

Antenna effects in truxene-bridged BODIPY triarylzinc(II)porphyrin dyads: evidence for a dual Dexter-Forster mechanism

期刊

DALTON TRANSACTIONS
卷 43, 期 22, 页码 8219-8229

出版社

ROYAL SOC CHEMISTRY
DOI: 10.1039/c3dt53630k

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资金

  1. Centre National de la Recherche Scientifique (ICMUB) [UMR CNRS 6302]
  2. CNRS
  3. Universite de Bourgogne
  4. Conseil Regional de Bourgogne through the 3MIM integrated project (Marquage de Molecules par les Metaux pour l'Imagerie Medicale)
  5. Agence Nationale de la Recherche (ANR)
  6. Sciences and Engineering Research Council of Canada (NSERC)

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The antenna process from an energy donor (BODIPY; 4',4'-difluoro-1',3',5',7'-tetramethyl-4'-bora- 3a',4a'-diaza-s-indacene) in its singlet state to two acceptors (two zinc(II) 5,15-p-tolyl-10- phenylporphyrin) bridged by a central truxene residue (5',5'',10',10'',15',15''-hexabutyltruxene), 5, has been analysed by means of comparison of the energy transfer rates with those of a structurally similar beta-substituted BODIPY-(zinc(II) 5,10,15-p-tolyl-porphyrin), 6, where no conjugation is present between the donor and the two acceptors using the Forster resonance energy transfer (FRET) approximation. It is estimated that the energy transfer in 5 operates mostly via a Dexter mechanism (>99%), and the remaining proceeds via a Forster mechanism (<1%). This information is useful for the design of future molecular devices aimed at harvesting light.

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