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D-π-A-π-D型小分子红光材料的制备及其性能

Design, Synthesis and Properties of D-π-A-π-D Type Organic Red Light Luminogens

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【作者】 贾钧森王飞赵波杨晶晶余春燕孙静王华许并社

【Author】 JIA Jun-sen;WANG Fei;ZHAO Bo;YANG Jing-jing;YU Chun-yan;SUN Jing;WANG Hua;XU Bing-she;Key Laboratory of Interface Science and Engineering in Advanced Materials,Ministry of Education,Taiyuan University of Technology;College of Materials Science and Engineering,Taiyuan University of Technology;Key Laboratory for Organic Electronics and Information Displays & Institute of Advanced Materials( IAM) ,Nanjing University of Posts & Telecommunications;

【通讯作者】 孙静;

【机构】 太原理工大学新材料界面科学与工程教育部重点实验室太原理工大学材料科学与工程学院南京邮电大学有机电子与信息显示国家重点实验室培育基地信息材料与纳米技术研究院

【摘要】 开发新型有机红光材料对于制备高性能红光有机电致发光器件具有重要的研究意义。本文采用SUZUKI偶联反应,以芴酮为受体(A)、3,4,5-三甲氧基苯为给体(D)合成了新型D-π-A-π-D结构的有机红光材料(3MeFO)。通过1H NMR谱、13C NMR谱和X单晶衍射确认了分子结构,该化合物展示了较强的电荷转移作用和良好的共轭结构,其晶体的发射峰达到620 nm。从单晶结构中看出甲氧基的引入有利于在分子间形成大量的氢键,有效地增强了分子间的相互作用。同时,该材料表现出良好的热稳定性能和电化学性能,使得其在OLED中展示了良好的电致发光性能。

【Abstract】 To develop a novel red light luminescent material was important to prepare the high-efficiency organic light emitting devices. In this paper, a new kind of D-π-A-π-D red light luminogen utilizing fluorenone as acceptor and 3,4,5-trimethoxybenzene as donor was designed and synthesized, named 3 MeFO. Its structure was confirmed by the 1H NMR spectra, 13C NMR spectra and X-ray single crystal diffraction. The compound had strong charge transfer and π-conjugated structure that contributed to the red shift and the PL peak of crystal was located at 620 nm. From the single crystal analysis, the introduction of methoxy groups had increased the intermolecular interaction owing to the formation of the hydrogen bond. Meanwhile, the compound exhibited excellent thermal stability properties, electrochemical performance that were benefit to prepare the OLED with the considerable electroluminescent properties.

【基金】 山西省高等学校科技创新项目;国家自然科学基金(61904120);山西省自然科学基金(201901D211090,201801D221124,201801D121101)资助项目~~
  • 【文献出处】 发光学报 ,Chinese Journal of Luminescence , 编辑部邮箱 ,2020年01期
  • 【分类号】TN383.1;TB34
  • 【被引频次】3
  • 【下载频次】185
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