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Donor–acceptor-structured 14-diazatriphenylene derivatives exhibiting thermally activated delayed fluorescence: design and synthesis photophysical properties and OLED characteristics

机译:供体-受体结构的14-二氮杂苯并菲衍生物具有热活化的延迟荧光:设计与合成光物理性质和OLED特性

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摘要

A new series of luminescent 1,4-diazatriphenylene (ATP) derivatives with various peripheral donor units, including phenoxazine, 9,9-dimethylacridane and 3-(diphenylamino)carbazole, is synthesized and characterized as thermally activated delayed fluorescence (TADF) emitters. The influence of the donor substituents on the electronic and photophysical properties of the materials is investigated by theoretical calculations and experimental spectroscopic measurements. These ATP-based molecules with donor–acceptor–donor (D–A–D) structures can reduce the singlet–triplet energy gap (0.04–0.26 eV) upon chemical modification of the ATP core, and thus exhibit obvious TADF characteristics in solution and doped thin films. As a demonstration of the potential of these materials, organic light-emitting diodes containing the D–A–D-structured ATP derivatives as emitters are fabricated and tested. External electroluminescence quantum efficiencies above 12% and 8% for green- and sky-blue-emitting devices, respectively, are achieved.
机译:合成了一系列新的发光的1,4-二氮杂三亚苯基(ATP)衍生物,其具有各种外围供体单元,包括吩恶嗪,9,9-二甲基rid啶和3-(二苯基氨基)咔唑,并被表征为热激活延迟荧光(TADF)发射体。通过理论计算和实验光谱测量研究了供体取代基对材料的电子和光物理性质的影响。这些具有供体-受体-供体(D–A–D)结构的基于ATP的分子可以在化学修饰ATP核心时减少单重态-三重态能隙(0.04-0.26 eV),因此在溶液和溶液中表现出明显的TADF特性。掺杂的薄膜。为了证明这些材料的潜力,制造并测试了包含D–A–D结构的ATP衍生物作为发射体的有机发光二极管。对于发射绿光和天蓝光的器件,外部电致发光量子效率分别达到12%和8%以上。

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