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首页> 外文期刊>Synthetic Metals >Synthesis, characterization, and photo- and electro-luminescence of new Ir(III) complexes with carrier transporting group-functionalized dibenzoylmethane ligand for green phosphorescent OLEDs
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Synthesis, characterization, and photo- and electro-luminescence of new Ir(III) complexes with carrier transporting group-functionalized dibenzoylmethane ligand for green phosphorescent OLEDs

机译:新型Ir(III)配合物的合成,表征以及光致发光和电致发光,用于绿色磷光OLED,具有载流子传输基团官能化的二苯甲酰甲烷配体

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Two new iridium(III) complexes containing the coumarin derivatives as cyclometalated ligands (L) and the carrier transporting group-functionalized dibenzoylmethane as ancillary ligands have been successfully synthesized and characterized. The X-ray crystal structure analyses of the free ligands and the complex containing a carbazole-functionalized dibenzoylmethane as ancillary ligand were described. The photophysical properties of the KIR) complexes were examined via ultraviolet-visible, photoluminescence spectroscopic spectra. The good thermal stability of the Ir(III) complexes was demonstrated by the thermogravimetric analysis. The doped light-emitting devices using the Ir(III) complexes as dopants were fabricated. The devices based on the complex containing a carbazole-functionalized dibenzoylmethane as ancillary ligand possess better performance as compared with the devices fabricated by the complex containing a 1,3,4-oxadiazole-functionalized dibenzoylmethane as ancillary ligand. The devices based on the former Ir(III) complex with a 15 wt% doping concentration exhibit a maximum efficiency of 13.8 cd/A and a maximum brightness of 4955.7 cd/m(2). (C) 2015 Elsevier B.V. All rights reserved.
机译:已经成功地合成和表征了两种新的铱(III)配合物,它们包含香豆素衍生物作为环金属化的配体(L)和载流子官能团的二苯甲酰甲烷作为辅助配体。描述了游离配体和含有咔唑官能化的二苯甲酰甲烷作为辅助配体的配合物的X射线晶体结构分析。通过紫外可见光致发光光谱检查了KIR)配合物的光物理性质。通过热重分析证明了Ir(III)配合物的良好热稳定性。制备了使用Ir(III)络合物作为掺杂剂的掺杂发光器件。与由含有1,3,4-恶二唑官能化的二苯甲酰甲烷作为辅助配体的配合物制造的装置相比,基于含有咔唑官能化的二苯甲酰甲烷作为辅助配体的配合物的装置具有更好的性能。基于具有15 wt%掺杂浓度的前Ir(III)配合物的器件显示出最大效率为13.8 cd / A,最大亮度为4955.7 cd / m(2)。 (C)2015 Elsevier B.V.保留所有权利。

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