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Highly fluorescent emitters based on triphenylamine‐π‐triazine (D‐π‐A) system: effect of extended conjugation on singlet‐triplet energy gap

Research output: Contribution to journalArticle

Author(s)

Shiv Kumar, Pachaiyappan Rajamalli, David B. Cordes, Alexandra M. Z. Slawin, Eli Zysman-Colman

School/Research organisations

Abstract

Three D‐π‐A type linearly‐extended emitters, based on diphenylamine (DPA ) as the donor and 2,4,6‐triphenyl‐1,3,5‐triazine (TRZ ) as the acceptor, were synthesized and their optoelectronic properties characterized. The introduction of an additional phenyl or phenylethynyl π‐spacer results in an enhancement of the molar extinction coefficient and a systematic bathochromic shift of the charge‐transfer transition in the absorption spectra. A mirrored bathochromic shift in the photoluminescence spectra is also observed with increasing conjugation of the bridge moiety. All three compounds show high photoluminescence quantum yields and moderate singlet‐triplet excited state energy gaps, ΔE ST, of 0.26‐0.37 eV were observed in 10 wt% doped films in mCP as the host matrix.
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Details

Original languageEnglish
Number of pages10
JournalAsian Journal of Organic Chemistry
VolumeEarly View
Early online date27 May 2020
DOIs
Publication statusE-pub ahead of print - 27 May 2020

    Research areas

  • Donor-acceptor, Charge transfer, Fluorescence, Thermally activated delayed fluorescence, Triazine

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