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作为基于热活化延迟荧光的有机发光二极管主体材料的芳基取代吖啶类化合物。

Aryl-substituted acridanes as hosts for TADF-based OLEDs.

作者信息

Masimukku Naveen, Gudeika Dalius, Bezvikonnyi Oleksandr, Syvorotka Ihor, Keruckiene Rasa, Volyniuk Dmytro, Grazulevicius Juozas V

机构信息

Department of Polymer Chemistry and Technology, Kaunas University of Technology, Radvilenu pl. 19, LT-50254, Kaunas, Lithuania.

Scientific Research Company "Electron-Carat", 202 Stryska Str. 79031, Lviv, Ukraine.

出版信息

Beilstein J Org Chem. 2020 May 13;16:989-1000. doi: 10.3762/bjoc.16.88. eCollection 2020.

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 cm/V·s at electric fields higher then ca. 2.5 × 10 V/cm. The selected compounds were used as hosts in electroluminescent devices which demonstrated maximum external quantum efficiencies up to 3.2%.

摘要

设计、合成并表征了四种芳基取代的吖啶衍生物,作为基于具有热激活延迟荧光发射体的有机发光二极管的电活性材料。这些化合物具有相对较高的热稳定性,玻璃化转变温度在79 - 97℃范围内。这些化合物在0.31 - 0.38 V范围内显示出源自吖啶基的氧化带。固体薄膜的电离势范围为5.39至5.62 eV。所开发的材料的三线态能量高于2.5 eV。10 - 乙基 - 9,9 - 二甲基 - 2,7 - 二(萘 - 1 - 基)- 9,10 - 二氢吖啶层在高于约2.5×10 V/cm的电场下显示出空穴迁移率达到10 cm²/V·s。所选化合物用作电致发光器件的主体,其最大外量子效率高达3.2%。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e97a/7237810/549550f7e530/Beilstein_J_Org_Chem-16-989-g008.jpg

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