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dc.contributor.advisorZysman-Colman, Eli
dc.contributor.authorWang, Jingxiang
dc.coverage.spatial316en_US
dc.date.accessioned2025-01-30T12:28:43Z
dc.date.available2025-01-30T12:28:43Z
dc.date.issued2025-07-03
dc.identifier.urihttps://hdl.handle.net/10023/31282
dc.description.abstractMulti-resonant thermally activated delayed fluorescence (MR-TADF) materials have been widely investigated as emitters in organic light-emitting diodes (OLEDs) due to their bright and narrowband emission that results from their rigid structures and short-range charge transfer (SRCT) character of the emissive excited state. However, their planar geometry and relatively large singlet-triplet energy gap lead to, respectively, severe aggregation-caused quenching (ACQ) and slow reverse intersystem crossing (RISC). This thesis is partially centered on developing new MR-TADF emitters to solve these two problems. Using chiral compounds that can emit circularly polarized luminescence (CPL) is beneficial for their potential to increase the light out-coupling efficiency of OLEDs that use anti-glare filters. This thesis also investigates the design of chiral MR-TADF emitters, aiming to achieve bright, narrowband emission showing a strong CPL signal. Chapter 1 introduces what is an OLED and how it works. The design of TADF emitters along with overviews of the development of heavy-atom-based MR-TADF emitters and chiral MR-TADF emitters are also discussed. Chapter 2 presents the design of two MR-TADF emitters, TPPO-tBu-DiKTa and TPA-tBu-DiKTa, and the effect of twisted peripheral groups on the alleviation of ACQ and improvement of RISC. Chapter 3 demonstrates two heavy-atom-based MR-TADF emitters, DiKTaSe and tBuCz-DiKTaSe, and the contribution of heavy atom effect to the TADF performance and efficiency roll-off in OLEDs. Chapter 4 describes two chiral MR-TADF emitters tBuPh-BN and DPA-tBuPh-BN and their TADF and chiroptical properties. Chapter 5 demonstrates the design of a propeller-shaped triple helicene DiKTa3 and explores its chiroptical properties through Density Functional Theory calculations. Chapter 6 reports the design of a series of TADF polymers. Their TADF performance is investigated. The formation of chiral phase in polymer film through blending with chiral additives and their chiroptical properties are explored. Chapter 7 includes the experimental methods used in this thesis.en_US
dc.description.sponsorship"This work was supported by China Scholarship Council (Grant number 202006250026) and the School of Chemistry at the University of St Andrews."--Fundingen
dc.language.isoenen_US
dc.relationData underpinning Jingxiang Wang's thesis, Wang, J., University of St Andrews, 23 Jan 2026, https://doi.org/10.17630/e87d5177-ca2b-40c3-9d92-f8a90371564b
dc.relation
dc.relationPoulard, L., Kasemthaveechok, S., Coehlo, M., Kumar, R. A., Frédéric, L., Sumsalee, P., d’Anfray, T., Wu, S., Wang, J., Matulaitis, T., Crassous, J., Zysman-Colman, E., Favereau, L., & Pieters, G. (2022). Circularly polarized-thermally activated delayed fluorescent materials based on chiral bicarbazole donors. Chemical Communications, Advance Article. Advance online publication. https://doi.org/10.1039/D2CC00998F
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dc.relationWang, J., Ortiz, J. S. O., McKay, A., Cordes, D. B., Crassous, J., & Zysman-Colman, E. (2024). A chiral propeller-shaped triple helicene shows multi-resonant thermally activated delayed fluorescence. Helvetica Chimica Acta, Early View, Article e202400129. Advance online publication. https://doi.org/10.1002/hlca.202400129
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dc.relationWang, J., Hafeez, H., Tang, S., Matulaitis, T., Edman, L., Samuel, I. D. W., & Zysman-Colman, E. (2024). Highly efficient organic light-emitting diodes and light-emitting electrochemical cells employing multiresonant thermally activated delayed fluorescent emitters with bulky donor or acceptor peripheral groups. Aggregate, Early View, Article e571. Advance online publication. https://doi.org/10.1002/agt2.571
dc.relation
dc.relationWu, S., Hu, Y.-N., Wang, J., Sun, D., Wang, K., Zhang, X.-H., & Zysman-Colman, E. (2024). Efficient orange organic light-emitting diodes employing a central aniline bridged multiresonant thermally activated delayed fluorescence emitter. Journal of Materials Chemistry C, 12(17), 6177-6184. https://doi.org/10.1039/D4TC00506F
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dc.relationMiranda-Salinas, H., Wang, J., Danos, A., Matulaitis, T., Stavrou, K., Monkman, A. P., & Zysman-Colman, E. (2024). Peripheral halogen atoms in multi-resonant thermally activated delayed fluorescence emitters: the role of heavy atom on intermolecular interactions and spin orbit coupling. Journal of Materials Chemistry C, 12(6), 1996-2006. https://doi.org/10.1039/D3TC04394K
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dc.relationWu, S., Zhang, L., Wang, J., Gupta, A. K., Samuel, I. D. W., & Zysman-Colman, E. (2023). Merging boron and carbonyl based MR-TADF emitter designs to achieve high performance pure blue OLEDs. Angewandte Chemie International Edition, 62(28), Article e202305182. https://doi.org/10.1002/anie.202305182
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dc.relationWang, J., Chen, D., Moreno-Naranjo, J. M., Zinna, F., Frédéric, L., Cordes, D. B., McKay, A., Fuchter, M. J., Zhang, X., & Zysman-Colman, E. (2024). Helically chiral multiresonant thermally activated delayed fluorescent emitters and their use in hyperfluorescent organic light-emitting diodes. Chemical Science, 15(41), 16917-16927. https://doi.org/10.1039/D4SC03478C
dc.relation.urihttps://doi.org/10.17630/e87d5177-ca2b-40c3-9d92-f8a90371564b
dc.relation.urihttps://doi.org/10.1039/D2CC00998F
dc.relation.urihttps://doi.org/10.1002/hlca.202400129
dc.relation.urihttps://doi.org/10.1002/agt2.571
dc.relation.urihttps://doi.org/10.1039/D4TC00506F
dc.relation.urihttps://doi.org/10.1039/D3TC04394K
dc.relation.urihttps://doi.org/10.1002/anie.202305182
dc.relation.urihttps://doi.org/10.1039/D4SC03478C
dc.rightsCreative Commons Attribution 4.0 International*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.subjectThermally activated delayed fluorescenceen_US
dc.subjectMulti-resonanten_US
dc.subjectOrganic light-emitting diodesen_US
dc.subjectCircularly polarized luminescenceen_US
dc.subjectChiral emitteren_US
dc.titleDesign and synthesis of multi-resonant thermally activated delayed fluorescence materials and chiral emittersen_US
dc.typeThesisen_US
dc.contributor.sponsorChina Scholarship Council (CSC)en_US
dc.contributor.sponsorUniversity of St Andrews. School of Chemistryen_US
dc.type.qualificationlevelDoctoralen_US
dc.type.qualificationnamePhD Doctor of Philosophyen_US
dc.publisher.institutionThe University of St Andrewsen_US
dc.rights.embargodate2026-01-23
dc.rights.embargoreasonThesis restricted in accordance with University regulations. Restricted until 23rd January 2026en
dc.identifier.doihttps://doi.org/10.17630/sta/1216
dc.identifier.grantnumber202006250026en_US


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