Carbazole Derivatives for Blue OLEDs

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  • Published: 14 July 2018
  • Copyright: Wiley-VCH Verlag GmbH & Co. KGaA
  • Source / Publisher: Chemical Communications/Royal Society of Chemistry
  • Associated Societies: Royal Society of Chemistry (RSC), UK
thumbnail image: Carbazole Derivatives for Blue OLEDs

Organic light-emitting diodes (OLEDs) are used in display technology.  Phosphorescent materials for such OLEDs have a higher theoretical efficiency than fluorescent materials, but finding phosphorescent materials for stable blue OLEDs is a challenge. An alternative is the use of so-called thermally activated delayed fluorescence (TADF) molecules, which also have high efficiencies.

Youichi Tsuchiya, Hajime Nakanotani, Chihaya Adachi, Kyushu University, Fukuoka, Japan, and colleagues have synthesized trifluoromethane-modified carbazole derivatives as stable blue TADF emitters. The team obtained the desired molecules by a SNAr reaction of tetrafluorophthalonitrile with CF3-modified carbazoles using sodium hydride in tetrahydrofuran (THF). The products were purified by sublimation.

The team found that the trifluoromethane groups induced a blue shift of about 40–55 nm in the compound's emission compared with hydrogen-substituted analogues. This was attributed to the electron-withdrawing nature of the CF3 groups. The modification also improved the photoluminescence yield and the stability. According to the researchers, these results show that CF3-modified carbazoles are promising for the development of stable, efficient, deep-blue emitting TADF molecules.


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