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Enhanced triplet formation by twisted intramolecular charge-transfer excited states in conjugated oligomers and polymers.

King, S.M.; Matheson, R.; Dias, F.B.; Monkman, A.P.

Authors

S.M. King

R. Matheson



Abstract

The triplet yield and intersystem crossing rate of a set of conjugated oligomers and polymers that, in polar solvents, form a charge-transfer state with a twisted conformation has been investigated. It was observed that in these dibenzothiophene-fluorene oligomers a greater than 10-fold increase on the triplet yield is achieved by simply changing the medium polarity to favor the formation of the twisted charge-transfer state, while the fluorescence lifetime is only slightly increased. The increase in the intersystem crossing rate is attributed to the improved mixing between the singlet and triplet states in the twisted excited state. In analogous polymers, the intersystem crossing rate does not show the same increase, most likely because of the greater energetic and conformational disorder increasing the intersystem crossing rate at all times, regardless of the formation of the twisted charge-transfer state or not.

Citation

King, S., Matheson, R., Dias, F., & Monkman, A. (2008). Enhanced triplet formation by twisted intramolecular charge-transfer excited states in conjugated oligomers and polymers. Journal of Physical Chemistry B (Soft Condensed Matter and Biophysical Chemistry), 112(27), 8010-8016. https://doi.org/10.1021/jp712163b

Journal Article Type Article
Publication Date 2008-07
Deposit Date Nov 3, 2010
Journal Journal of Physical Chemistry B (Soft Condensed Matter and Biophysical Chemistry)
Print ISSN 1520-6106
Electronic ISSN 1520-5207
Publisher American Chemical Society
Peer Reviewed Peer Reviewed
Volume 112
Issue 27
Pages 8010-8016
DOI https://doi.org/10.1021/jp712163b
Public URL https://durham-repository.worktribe.com/output/1537650