Excited State Dynamics of Thermally Activated Delayed Fluorescence from an Excited State Intramolecular Proton Transfer System

Yun Long, Masashi Mamada, Chunyong Li, Paloma Lays Dos Santos, Marco Colella, Andrew Danos, Chihaya Adachi, Andrew Monkman

研究成果: Contribution to journalArticle査読

10 被引用数 (Scopus)

抄録

We describe the photophysical processes that give rise to thermally activated delayed fluorescence in the excited state intramolecular proton transfer (ESIPT) molecule, triquinolonobenzene (TQB). Using transient absorption and time-resolved photoluminescence spectroscopy, we fully characterize prompt and delayed emission, phosphorescence, and oxygen quenching to reveal the reverse intersystem crossing mechanism (rISC). After photoexcitation and rapid ESIPT to the TQB-TB tautomer, emission from S1 is found to compete with thermally activated ISC to an upper triplet state, T2, very close in energy to S1 and limiting photoluminescence quantum yield. T2 slowly decays to the lowest triplet state, T1, via internal conversion. In the presence of oxygen, T2 is quenched to the ground state of the double proton transferred TQB-TC tautomer. Our measurements demonstrate that rISC in TQB occurs from T2 to S1 driven by thermally activated reverse internal conversion from T1 to T2 and support recent calculations by Cao et al. (Cao, Y.; Eng, J.; Penfold, T. J. Excited State Intramolecular Proton Transfer Dynamics for Triplet Harvesting in Organic Molecules. J. Phys. Chem. A 2019, 123, 2640-2649).

本文言語英語
ページ(範囲)3305-3312
ページ数8
ジャーナルJournal of Physical Chemistry Letters
11
9
DOI
出版ステータス出版済み - 5 7 2020

All Science Journal Classification (ASJC) codes

  • 材料科学(全般)
  • 物理化学および理論化学

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