Skip to main content

Research Repository

Advanced Search

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.

Intramolecular locking and coumarin insertion: a stepwise approach for TADF design Thumbnail


Authors

S. Paredis

T. Cardeynaels

S. Brebels

J. Deckers

Suman Kuila suman.kuila@durham.ac.uk
Post Doctoral Research Associate

A. Lathouwers

M. Van Landeghem

K. Vandewal

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

Files






You might also like



Downloadable Citations