Haykir, Gulcin and Aydemir, Murat and Danos, Andrew and Gumus, Selcuk and Hizal, Gurkan and Monkman, Andrew P. and Turksoy, Figen (2021) 'Effects of asymmetric acceptor and donor positioning in deep blue pyridyl-sulfonyl based TADF emitters.', Dyes and pigments., 194 . p. 109579.
In this work, we report synthesis and photophysical properties of deep-blue emitting donor-acceptor (D-A) and donor-acceptor-donor (D-A-D) thermally activated delayed fluorescence (TADF) molecules, where the molecules designed using carbazole as a donor (D) and a pyridyl (a)-sulfonyl (A) based bifunctional group as an acceptor. The work reveals how structural changes favor reverse intersystem crossing (rISC) by forming emissive charge transfer (CT) state, which is thoroughly investigated in different donor and asymmetric acceptor positions. Three comparison sets of regioisomers are investigated. 2,5-substituted pyridine derivatives in Set-1, are D-Aa, D-aA and D-Aa-D structures with asymmetric acceptor systems, revealing that the donor nearer to the pyridine group substantially controls the TADF properties In Set-2, modified the D-Aa-D structures reveal how ortho and meta positioned a relative to A (keeping the carbazole at meta to the A) affects the emission properties, deactivating TADF and promotion triplet-triplet annihilation. In the final set, 2,4-substituted pyridyl-sulfonyl derivatives show that the positioning of the donor far from the pyridine group has minimal influence. This final set of molecules show superior optical and physical properties though, indicating the importance of correct positioning between D, a, and A.
|Full text:||Publisher-imposed embargo until 02 July 2023. |
(AM) Accepted Manuscript
Available under License - Creative Commons Attribution Non-commercial No Derivatives 4.0.
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|Publisher Web site:||https://doi.org/10.1016/j.dyepig.2021.109579|
|Publisher statement:||© 2021 This manuscript version is made available under the CC-BY-NC-ND 4.0 license http://creativecommons.org/licenses/by-nc-nd/4.0/|
|Date accepted:||16 June 2021|
|Date deposited:||22 July 2021|
|Date of first online publication:||02 July 2021|
|Date first made open access:||02 July 2023|
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