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A facile way to synthesize high-triplet-energy hosts for blue phosphorescent organic light-emitting diodes with high glass transition temperature and low driving voltage

机译:合成具有高玻璃化转变温度和低驱动电压的蓝色磷光有机发光二极管的高三重态能量主体的简便方法

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摘要

Two novel bipolar host materials were designed and synthesized, by incorporating a-carboline and carbazole to spiro-acridine-fluorene skeleton. As expected, both materials exhibited high triplet energy over 2.8 eV, indicating they could act as suitable blue hosts in phosphorescent organic light-emitting diodes. By changing the appending group from carbazole to alpha-carboline, the thermal property and molecular bipolarity were improved. When they were applied as hosts for sky-blue emitter iridium(III) bis[4,6-difluorophenyl]pyridinato-N, C2' ] picolinate (FIrpic), good performance of 35.5 cd A(-1), 35.8 lm W-1 and 29.5 cd A(-1), 24.5 lm W-1 was achieved for alpha-carboline derivative and carbazole derivative, respectively. (C) 2015 Elsevier Ltd. All rights reserved.
机译:通过将α-咔啉和咔唑结合到螺-啶芴骨架上,设计并合成了两种新型的双极性主体材料。正如预期的那样,两种材料均显示出超过2.8 eV的高三重态能量,表明它们可以充当磷光有机发光二极管中的合适蓝色主体。通过将连接基团从咔唑改为α-咔啉,可改善热性质和分子双极性。当将它们用作天蓝色发射体铱(III)双[4,6-二氟苯基]吡啶基-N,C2']吡啶甲酸(FIrpic)的基质时,具有35.5 cd A(-1),35.8 lm W-对于α-咔啉衍生物和咔唑衍生物,分别获得1和29.5 cd A(-1),达到24.5 lm W-1。 (C)2015 Elsevier Ltd.保留所有权利。

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