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Influence of chain length on exciton migration to low-energy sites in single fluorene copolymers

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Abstract

Fluorescence spectroscopy was performed on single molecules of two 9,9-dialkylfluorene–benzothiadazole (FxBT) copolymers with a 10-fold difference in average molecular weight. Molecules of both polymers exhibit red-shifted emission indicative of energy migration to low-energy sites (LES) on the polymer chains; however, “red” spectra are much more common for the longer polymer. Since singlet-exciton migration is found to occur on the molecular length scale in both cases, the increased number of red-shifted spectra observed for the longer polymer is evidence that the likelihood of LES formation increases with chain length. This relationship is discussed in terms of three possible causes of low-energy sites: local polymer conformations, chromophores with extended conjugation lengths, and random chemical defects.

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Authors and Affiliations

  1. Department of Chemistry and Biochemistry, Center for Nano and Molecular Science and Technology, The University of Texas at Austin, Austin, TX 78712-1062, USA

    Robin K. Lammi & Paul F. Barbara

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  1. Robin K. Lammi
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  2. Paul F. Barbara
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Correspondence to Paul F. Barbara.

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Dedicated to Professor Hiroshi Masuhara on the occasion of his 60th birthday

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Lammi, R.K., Barbara, P.F. Influence of chain length on exciton migration to low-energy sites in single fluorene copolymers. Photochem Photobiol Sci 4, 95–99 (2005). https://doi.org/10.1039/b417753n

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  • DOI: https://doi.org/10.1039/b417753n

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