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通用直接环化构建用于高效热激活延迟荧光发射体的螺吖啶衍生物。

Versatile Direct Cyclization Constructs Spiro-acridan Derivatives for Highly Efficient TADF emitters.

作者信息

Liu He, Liu Zhiwen, Li Ganggang, Huang Huaina, Zhou Changjiang, Wang Zhiming, Yang Chuluo

机构信息

College of Materials Science and Engineering, Shenzhen University, Shenzhen, 518055, P. R. China.

State Key Laboratory of Luminescent Materials and Devices, Center for Aggregation-Induced Emission, Guangzhou International Campus, South China University of Technology (SCUT), Guangzhou, 510640, P. R. China.

出版信息

Angew Chem Int Ed Engl. 2021 May 25;60(22):12376-12380. doi: 10.1002/anie.202103187. Epub 2021 Apr 28.

Abstract

Spiro-acridan (SpA) derivatives possess a great potential in preparing efficient thermally activated delayed fluorescent (TADF) emitters. However, the conventional synthetic routes are cost-expensive and time-consuming. The development of a simple procedure to synthesize SpAs is still in urgent pursuing appreciated by academic and industrial communities. In this contribution, we present a feasible acid-catalyzed solvent-free metal-free cyclization between diarylamines and ketones to construct SpAs. The as-constructed moieties provide a wide possibility to assemble efficient TADF emitters. As an example, D2T-TR with high photoluminescent quantum yield and proper TADF character is applied in organic light emitting diodes (OLEDs) which achieves a maximum external quantum efficiency (EQE) of 27.1 %. This work shows us a bright inspiration on developing excellent organic optoelectronic materials and an effective tool to realize it.

摘要

螺吖啶(SpA)衍生物在制备高效热激活延迟荧光(TADF)发光体方面具有巨大潜力。然而,传统的合成路线成本高昂且耗时。开发一种简单的合成SpA的方法仍然是学术界和工业界迫切追求的目标。在本论文中,我们提出了一种可行的酸催化无溶剂无金属的二芳基胺与酮之间的环化反应来构建SpA。所构建的部分为组装高效TADF发光体提供了广泛的可能性。例如,具有高光致发光量子产率和适当TADF特性的D2T-TR被应用于有机发光二极管(OLED)中,其最大外量子效率(EQE)达到了27.1%。这项工作为开发优秀的有机光电子材料向我们展示了一个光明的灵感,以及实现它的有效工具。

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