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Aryl-substituted acridanes as hosts for TADF-based OLEDs

  • Naveen Masimukku
  • , Dalius Gudeika
  • , Oleksandr Bezvikonnyi
  • , Ihor Syvorotka
  • , Rasa Keruckiene
  • , Dmytro Volyniuk
  • , Juozas V. Grazulevicius*
  • *Corresponding author for this work
  • Kaunas University of Technology
  • Scientific Research Company

Research output: Contribution to journal › Article › peer-review

2 Citations (Scopus)

Abstract

Four aryl-substituted acridan derivatives were designed, synthesized and characterized as electroactive materials for organic light emitting diodes based on emitters exhibiting thermally activated delayed fluorescence. These compounds possessed relatively high thermal stability with glass-transition temperatures being in the range of 79-97 °C. The compounds showed oxidation bands arising from acridanyl groups in the range of 0.31-038 V. Ionization potentials of the solid films ranged from 5.39 to 5.62 eV. The developed materials were characterized by triplet energies higher than 2.5 eV. The layer of 10-ethyl-9,9-dimethyl-2,7-di(naphthalen- 1-yl)-9,10-dihydroacridine demonstrated hole mobilities reaching10-3 cm2/V·s at electric fields higher then ca. 2.5 × 105 V/cm. The selected compounds were used as hosts in electroluminescent devices which demonstrated maximum external quantum efficiencies up to 3.2%.

Original languageEnglish
Pages (from-to)989-1000
Number of pages12
JournalBeilstein Journal of Organic Chemistry
Volume16
DOIs
Publication statusPublished - 13 May 2020
Externally publishedYes

Keywords

  • Acridan
  • Hole mobility
  • Host
  • OLED
  • Thermally activated delayed fluorescence

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