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Updated: Jan 11, 2026

Scale-up Chemical Synthesis of Thermally-activated Delayed Fluorescence Emitters Based on the Dibenzothiophene-S,S-Dioxide Core
Published on: October 24, 2017
Stepwise Emission Tuning of Thermally Activated Delayed Fluorescence Emitters from the Orange to Near-Infrared Region
Shantaram Kothavale1, Rajendra Kumar Konidena2, Hyunjung Lee1
1School of Chemical Engineering, Sungkyunkwan University 2066 Seobu-ro, Jangan-gu, Suwon, Gyeonggi 16419, Korea.
Abstract:
Herein, we unveiled a rational molecular design to develop rigid and strong acceptors through interlocking followed by cyano substitution to tune the emission wavelength of thermally activated delayed fluorescence emitters from the orange (∼605 nm) to near-infrared (∼777 nm) region. Interlocking phenyl units in the 4,4'-(quinoxaline-2,3-diyl)dibenzonitrile core, paired with multicarbazole donors, resulted in a 70 nm red shift in emission. Further cyano substitution at the C2 and C7 positions of the dibenzo[a,c]phenazine-3,6-dicarbonitrile acceptor induced an additional 102 nm red shift. Consequently, organic light-emitting diodes with an emission wavelength range from orange to deep red were fabricated with an external quantum efficiency of >10%.
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