Spectroscopy and Transport of the Triplet Exciton in a Terthiophene End-Capped Poly(phenylene ethynylene)

Alison M. Funston, Eric E. Silverman, Kirk S. Schanze,§ and John R. Miller*
Chemistry Department, Brookhaven National Laboratory, Upton, New York, 11973-5000, and Department of Chemistry, University of Florida, PO Box 117200, Gainesville, Florida 32611-7200
J. Phys. Chem. B, 2006, 110 (36), pp 17736–17742
DOI: 10.1021/jp061114l
Publication Date (Web): August 18, 2006
Copyright © 2006 American Chemical Society

Abstract

Triplet states of poly(phenylene ethynylene), 3PPE*, not easily formed by direct photoexcitation, were produced by pulse radiolysis in toluene, along with triplet states of T3PPE having terthiophene end-caps. Intense triplet−triplet absorption maxima, ε680(3PPE*) = 9.5 × 104 M-1 cm-1 and ε780(3T3PPE*) = 2.8 × 104 M-1 cm-1 enable identification of these two species, which have triplet energies of 2.12 and 1.77 eV determined in bimolecular energy transfer equilibria. Bleaching of ground-state absorption measures 3PPE* to be the delocalized over a 1.8-nm length. Triplet states formed in the PPE chains were transported to and trapped by the end caps in a time 5 ns.

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History

  • Published In Issue September 14, 2006
  • Received February 21, 2006
    Revised May 16, 2006

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