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Carbazole‐Based DABNA Analogues as Highly Efficient Thermally Activated Delayed Fluorescence Materials for Narrowband Organic Light‐Emitting Diodes

Susumu Oda, Wataru Kumano, Toshiki Hama, Ryosuke Kawasumi, Kazuki Yoshiura, Takuji Hatakeyama

2020Angewandte Chemie74 citationsDOI

Abstract

Abstract Carbazole‐based DABNA analogues ( CzDABNA s) were synthesized from triarylamine by regioselective one‐shot single and double borylation. The reaction proceeded selectively at the ortho position of the carbazolyl group, where the highest occupied molecular orbital is mainly localized owing to the difference in the electron‐donating abilities of the diarylamino and carbazolyl groups. The facile and scalable method enabled synthesis of CzDABNA s, exhibiting narrowband thermally activated delayed fluorescence with emission spectra ranging from deep blue to green. The organic light‐emitting diode devices employing these products as emitters exhibited deep‐blue, sky‐blue, and green emission with high external quantum efficiencies of 19.5, 21.8, and 26.7 %, respectively.

Topics & Concepts

CarbazoleRegioselectivityPhotochemistryFluorescenceOLEDChemistryDiodeMaterials scienceOptoelectronicsOrganic chemistryCatalysisOpticsPhysicsLayer (electronics)Organic Light-Emitting Diodes ResearchLuminescence and Fluorescent MaterialsOrganoboron and organosilicon chemistry
Carbazole‐Based DABNA Analogues as Highly Efficient Thermally Activated Delayed Fluorescence Materials for Narrowband Organic Light‐Emitting Diodes | Litcius