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Conjugated and nonconjugated bipolar-transporting dinuclear europium(III) complexes involving triphenylamine and oxadiazole units: Synthesis, photophysical and electroluminescent properties

机译:含三苯胺和恶二唑单元的共轭和非共轭双极传输双核di(III)配合物:合成,光物理和电致发光性质

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摘要

Two novel bipolar-transporting dinuclear europium(III) complexes incorporating both hole-transporting triphenylamine (TPA) and electron-transporting oxadiazole (OXD) units into the dual phenanthroline ligands were successfully synthesized and characterized by IR, elemental analysis, electrochemical, photophysical analysis, and thermogravimetric analysis, in which the OXD unit was attached onto TPA unit by conjugated and unconjugated linkages for the europium complex A and B, respectively. Compared with complex B, complex A exhibited higher thermal stability and quantum efficiency. A maximum brightness of 296.3 cd/m~2 at voltage of 8.5 V was obtained in the complex A-doped devices with saturated red emission using a blend of poly(vinylcarbazole) and 2-(4-biphenyl)-5-(4-tert-butyl-phenyl)-1,3,4- oxadiazole as a host matrix, which is about two-times higher than that from the complex B-doped devices with the same configuration. To best of our knowledge, this is one of the best results based on the dinuclear europium(III) complexes by spin-casting method.
机译:成功地合成了两种新型的双极传输双核di(III)配合物,将空穴传输的三苯胺(TPA)和电子传输的恶二唑(OXD)单元结合到双菲咯啉双配体中,并通过红外,元素分析,电化学,光物理分析,热重分析,其中OXD单元分别通过for配合物A和B的共轭和非共轭键连接到TPA单元上。与配合物B相比,配合物A表现出更高的热稳定性和量子效率。使用聚(乙烯基咔唑)和2-(4-联苯基)-5-(4-叔丁基苯基)-1,3,4-恶二唑作为主体基质,比具有相同配置的复杂B掺杂器件的两倍高。据我们所知,这是基于双核euro复合物通过旋转浇铸法的最佳结果之一。

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