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Synthesis and properties of oligofluorene-thiophenes as emissive materials for organic electroluminescent devices: Color-tuning from deep blue to orange

机译:低聚芴噻吩作为有机电致发光器件的发光材料的合成和性能:从深蓝色变为橙色

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摘要

A series of oligofluorene-thiophenes end-capped with 3,6-di-tert- butylcarbazole and pyrene were designed and synthesized for application as color tunable emissive materials for organic electroluminescent devices. They were characterized by 1H NMR, 13C NMR, FT-IR, UV-vis, PL spectroscopy, and mass spectrometry. Theoretical calculations revealed that the carbazole moiety attached to the end of the molecule is nearly perpendicular to oligofluorene-thiophene-pyrene plane and π-electrons in the ground state delocalize over the entire molecule. Their optical, thermal, and electrochemical properties could be tuned by varying the number of thiophene units in the molecule. All were electrochemically and thermally stable molecules. OLED devices of these materials emitted brightly in various colors from deep blue to orange. Particularly, deep blue (CIE coordinates of 0.16, 0.14) and green (CIE coordinates of 0.27, 0.61) devices showed high color quality close to the NTSC standards with high luminance efficiencies of 1.14 and 11.15 cd/A, respectively.
机译:设计并合成了一系列被3,6-二叔丁基咔唑和pyr封端的低聚芴噻吩,用作有机电致发光器件的颜色可调发射材料。它们的特征在于1 H NMR,13 C NMR,FT-IR,UV-vis,PL光谱和质谱。理论计算表明,附着在分子末端的咔唑部分几乎垂直于低聚芴-噻吩-py平面,基态的π电子在整个分子上分散。可以通过改变分子中噻吩单元的数量来调节其光学,热和电化学性质。所有都是电化学和热稳定分子。这些材料的OLED器件发出各种颜色的明亮光,从深蓝色到橙色。特别是深蓝色(CIE坐标为0.16、0.14)和绿色(CIE坐标为0.27、0.61)设备显示了接近NTSC标准的高色彩质量,分别具有1.14和11.15 cd / A的高亮度效率。

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