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Scale-up Chemical Synthesis of Thermally-activated Delayed Fluorescence Emitters Based on the Dibenzothiophene-S,S-Dioxide Core
Published on: October 24, 2017
Highly effective organic light-emitting diodes containing thermally activated delayed fluorescence emitters with
Chan Hee Lee1, Shin Hyung Choi1, Sung Joon Oh1
1Department of Energy and Materials Engineering, Dongguk University Seoul 04620 Republic of Korea saeyounlee@dongguk.edu.
Abstract:
In this study, we report new thermally activated delayed fluorescence (TADF) emitters, AcPYM (10,10'-(pyrimidine-2,5-diylbis(4,1-phenylene))bis(9,9-dimethyl-9,10-dihydroacridine)) and PxPYM (10,10'-(pyrimidine-2,5-diylbis(4,1-phenylene))bis(10H-phenoxazine)), by employing donor units at the 2,5-positions of the pyrimidine acceptor unit. The donor-acceptor-donor (D-A-D) units combined in the linear molecular structure of AcPYM or PxPYM enhanced the horizontally oriented alignment, and the horizontal transition dipole moments were realized by up to 87% in the host matrix. Organic light-emitting diodes (OLEDs) containing AcPYM and PxPYM emitters realized external quantum efficiencies (η ext) of 16.8% for blue and green emissions.
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