A Direct Arylation Approach toward Thermally Activated Delayed Fluorescence-Active Benzo[ <i>c</i> ][1,2,5]thiadiazole Emitters for Near-Infrared Solution-Processed OLEDs

An isomeric emitter (<b>2TPA-iCNBT</b>) is designed and synthesized, displaying enhanced thermally activated delayed fluorescence (TADF) properties as compared to the reference near-infrared (NIR) emitter TPACNBz (hereafter referred to as <b>2TPA-CNBT</b>). Its modified benzo-[<i>c</i>]-[1,2,5]-thiadiazole-4,7-dicarbonitrile (<b>iCNBT</b>) acceptor (A) core positions the two triphenylamine (TPA) donor (D) units adjacently, thereby increasing the D-A torsion angle. Synthesis is realized through the use of an unexploited direct arylation strategy, which, besides offering the desired materials in an efficient and straightforward way, can also yield monofunctionalized emitters (<b>1TPA-CNBT</b> and <b>1TPA-iCNBT</b>). In total, four emitters are synthesized, characterized, and subsequently compared in terms of their spectroscopic and device properties. Density functional theory is applied to simulate their relative molecular geometry and the arrangement of their (emissive) excited states. Steady-state and time-resolved emission spectroscopy reveal strongly contrasting TADF properties, with <b>2TPA-iCNBT</b> exhibiting the largest increase in the photoluminescence quantum yield on removal of oxygen (from 27 to 55%), and the fastest TADF emission kinetics in doped films (<i>k</i> <sub>RISC</sub> ∼ 10<sup>5</sup> s<sup>-1</sup>). In solution-processed organic light-emitting diodes, decent maximum external quantum efficiency (EQE) values are obtained for <b>2TPA-iCNBT</b> (2.49%), <b>1TPA-CNBT</b> (2.91%), and <b>1TPA-iCNBT</b> (2.76%), in clear contrast to <b>2TPA-CNBT</b> (1.16%), highlighting the decisive role of the D-A substitution pattern (and the number of D groups) on the performance of NIR-TADF emitters. Furthermore, <b>2TPA-iCNBT</b> is shown to maintain the highest EQE at larger current densities (EQE = 1.98% at 10 mA cm<sup>-2</sup>) within the investigated series, a consequence of its standout TADF behavior.

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Journal
ACS Applied Optical Materials
Published
2025-10-20
DOI
https://doi.org/10.1021/acsaom.5c00340
Primary Topic
Organic Light-Emitting Diodes Research
Type
article
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article

A Direct Arylation Approach toward Thermally Activated Delayed Fluorescence-Active Benzo[ c ][1,2,5]thiadiazole Emitters for Near-Infrared Solution-Processed OLEDs

Tom Cardeynaels, Koen Vandewal, Wouter Maes, Sonny Brebels et al.
ACS Applied Optical Materials
Organic Light-Emitting Diodes Research
article

A Direct Arylation Approach toward Thermally Activated Delayed Fluorescence-Active Benzo[ c ][1,2,5]thiadiazole Emitters for Near-Infrared Solution-Processed OLEDs

Tom Cardeynaels, Koen Vandewal, Wouter Maes, Sonny Brebels, Andrew Danos, Andrew P. Monkman, Melissa Van Landeghem, Benoı̂t Champagne, Emma V. Puttock, Huguette Penxten, Lucy Weatherill, Kamile Bareikaite
article en

Abstract

An isomeric emitter (<b>2TPA-iCNBT</b>) is designed and synthesized, displaying enhanced thermally activated delayed fluorescence (TADF) properties as compared to the reference near-infrared (NIR) emitter TPACNBz (hereafter referred to as <b>2TPA-CNBT</b>). Its modified benzo-[<i>c</i>]-[1,2,5]-thiadiazole-4,7-dicarbonitrile (<b>iCNBT</b>) acceptor (A) core positions the two triphenylamine (TPA) donor (D) units adjacently, thereby increasing the D-A torsion angle. Synthesis is realized through the use of an unexploited direct arylation strategy, which, besides offering the desired materials in an efficient and straightforward way, can also yield monofunctionalized emitters (<b>1TPA-CNBT</b> and <b>1TPA-iCNBT</b>). In total, four emitters are synthesized, characterized, and subsequently compared in terms of their spectroscopic and device properties. Density functional theory is applied to simulate their relative molecular geometry and the arrangement of their (emissive) excited states. Steady-state and time-resolved emission spectroscopy reveal strongly contrasting TADF properties, with <b>2TPA-iCNBT</b> exhibiting the largest increase in the photoluminescence quantum yield on removal of oxygen (from 27 to 55%), and the fastest TADF emission kinetics in doped films (<i>k</i> <sub>RISC</sub> ∼ 10<sup>5</sup> s<sup>-1</sup>). In solution-processed organic light-emitting diodes, decent maximum external quantum efficiency (EQE) values are obtained for <b>2TPA-iCNBT</b> (2.49%), <b>1TPA-CNBT</b> (2.91%), and <b>1TPA-iCNBT</b> (2.76%), in clear contrast to <b>2TPA-CNBT</b> (1.16%), highlighting the decisive role of the D-A substitution pattern (and the number of D groups) on the performance of NIR-TADF emitters. Furthermore, <b>2TPA-iCNBT</b> is shown to maintain the highest EQE at larger current densities (EQE = 1.98% at 10 mA cm<sup>-2</sup>) within the investigated series, a consequence of its standout TADF behavior.

ACS Applied Optical MaterialsVol. 3(11)
University of Namur (BE), Queen Mary University of London (GB), Durham University (GB), Imec the Netherlands (NL), Hasselt University (BE)
European Commission, Fonds De La Recherche Scientifique - FNRS, Fonds Wetenschappelijk Onderzoek, Vlaamse regering, Université de Namur
Openalex Percentile: Top 70%
Organic Light-Emitting Diodes Research
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