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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

Kumar, S and Rajamalli, P and Cordes, DB and Slawin, AMZ and Zysman-Colman, E (2020) Highly Fluorescent Emitters Based on Triphenylamine-π-Triazine (D-π-A) System: Effect of Extended Conjugation on Singlet-Triplet Energy Gap. In: Asian Journal of Organic Chemistry, 9 (9). pp. 1277-1285.

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Official URL: https://dx.doi.org/10.1002/ajoc.202000165

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, ΔEST, of 0.26-0.37 eV were observed in 10 wt doped films in mCP as the host matrix.

Item Type: Journal Article
Publication: Asian Journal of Organic Chemistry
Publisher: Wiley-VCH Verlag
Additional Information: Copy right for this article belongs to Wiley-VCH Verlag
Keywords: donor-acceptor charge transfer fluorescence thermally activated delayed fluorescence triazine
Department/Centre: Division of Chemical Sciences > Materials Research Centre
Date Deposited: 11 Dec 2020 11:55
Last Modified: 08 Dec 2022 11:34
URI: https://eprints.iisc.ac.in/id/eprint/65653

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