S. Paredis
Intramolecular locking and coumarin insertion: a stepwise approach for TADF design
Paredis, S.; Cardeynaels, T.; Brebels, S.; Deckers, J.; Kuila, S.; Lathouwers, A.; Van Landeghem, M.; Vandewal, K.; Danos, A.; Monkman, A. P.; Champagne, B.; Maes, W.
Authors
T. Cardeynaels
S. Brebels
J. Deckers
Suman Kuila suman.kuila@durham.ac.uk
Post Doctoral Research Associate
A. Lathouwers
M. Van Landeghem
K. Vandewal
Dr Andrew Danos andrew.danos@durham.ac.uk
Senior Experimental Officer
Professor Andrew Monkman a.p.monkman@durham.ac.uk
Professor
B. Champagne
W. Maes
Abstract
Three novel TADF (thermally activated delayed fluorescence) emitters based on the well-studied Qx-Ph-DMAC fluorophore are designed and synthesized. The photophysical properties of these materials are studied from a theoretical and experimental point of view, demonstrating the cumulative effects of multiple small modifications that combine to afford significantly improved TADF performance. First, an extra phenyl ring is added to the acceptor part of Qx-Ph-DMAC to increase the conjugation length, resulting in BQx-Ph-DMAC, which acts as an intermediate molecular structure. Next, an electron-deficient coumarin unit is incorporated to fortify the electron accepting ability, affording ChromPy-Ph-DMAC with red-shifted emission. Finally, the conjugated system is further enlarged by ‘locking’ the molecular structure, generating DBChromQx-DMAC with further red-shifted emission. The addition of the coumarin unit significantly impacts the charge-transfer excited state energy levels with little effect on the locally excited states, resulting in a decrease of the singlet–triplet energy gap. As a result, the two coumarin-based emitters show considerably improved TADF performance in 1 w/w% zeonex films when compared to the initial Qx-Ph-DMAC structure. ‘Locking’ the molecular structure further lowers the singlet–triplet energy gap, resulting in more efficient reverse intersystem crossing and increasing the contribution of TADF to the total emission.
Citation
Paredis, S., Cardeynaels, T., Brebels, S., Deckers, J., Kuila, S., Lathouwers, A., Van Landeghem, M., Vandewal, K., Danos, A., Monkman, A. P., Champagne, B., & Maes, W. (2023). Intramolecular locking and coumarin insertion: a stepwise approach for TADF design. Physical Chemistry Chemical Physics, 25(43), 29842-29849. https://doi.org/10.1039/d3cp03695b
Journal Article Type | Article |
---|---|
Acceptance Date | Oct 17, 2023 |
Online Publication Date | Oct 18, 2023 |
Publication Date | Nov 21, 2023 |
Deposit Date | Oct 30, 2023 |
Publicly Available Date | Oct 30, 2023 |
Journal | Physical Chemistry Chemical Physics |
Print ISSN | 1463-9076 |
Electronic ISSN | 1463-9084 |
Publisher | Royal Society of Chemistry |
Peer Reviewed | Peer Reviewed |
Volume | 25 |
Issue | 43 |
Pages | 29842-29849 |
DOI | https://doi.org/10.1039/d3cp03695b |
Public URL | https://durham-repository.worktribe.com/output/1863116 |
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his article is licensed under a Creative Commons Attribution 3.0 Unported Licence
Published Journal Article
(2.5 Mb)
PDF
Publisher Licence URL
http://creativecommons.org/licenses/by/3.0/
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