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Scale-up Chemical Synthesis of Thermally-activated Delayed Fluorescence Emitters Based on the Dibenzothiophene-S,S-Dioxide Core
Published on: October 24, 2017
Recent Progress of Novel Organic Near-Infrared-Emitting Materials
Ming-Peng Zhuo1,2, Xue-Dong Wang1, Liang-Sheng Liao1,3
1Institute of Functional Nano & Soft Materials (FUNSOM) Jiangsu Key Laboratory for Carbon-Based Functional Materials & Devices Soochow University Suzhou 215123 China.
Abstract:
Organic near-infrared (NIR) emissive materials integrating the intrinsic NIR light advantages and organic semiconductor characters have generated immense scientific interest in fundamental science and practical application, including optical communications, night vision, surveillance, and biomedical applications. Nevertheless, the intrinsic energy gap law engenders a huge challenge to simultaneously meet longer emission wavelength and higher luminescence efficiency for organic NIR emitters. Herein, it is suggested that the purposefully molecular design and crystal engineering for novel organic NIR materials are urgently studied and explored. Herein, recent advances in novel organic NIR materials, mainly focusing on the hybridized local and charge transfer (HLCT) compounds, thermally activated delayed fluorescence (TADF) emitters, CT cocrystals, neutral π-radicals, and excited-state intramolecular proton transfer (ESIPT)-active materials, are summarized. It is hoped that this perspective can afford a new insight into the fine design and synthesis of the desired organic NIR emitters.

