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稠环修饰的吩噻嗪类有机余辉体系:构筑策略与性能调控

刘佩佩,闫婉婷,袁文涛,李倩倩,李振   

  1. 武汉大学化学与分子科学学院
  • 收稿日期:2025-12-22 修回日期:2026-01-20 网络首发:2026-01-21 发布日期:2026-01-21
  • 通讯作者: 李倩倩 E-mail:liqianqian@whu.edu.cn
  • 基金资助:
    国家自然科学基金委 (批准号:22235006)资助

Engineering Fused-Ring Phenothiazine Systems: Strategies for Constructing and Tuning Organic Afterglow

LIU Peipei#, YAN Wanting#, YUAN Wentao, LI Qianqian*, LI Zhen*   

  1. Hubei Key Lab on Organic and Polymeric Opto-Electronic Materials, Department of Chemistry, Wuhan University
  • Received:2025-12-22 Revised:2026-01-20 Online First:2026-01-21 Published:2026-01-21
  • Supported by:
    Supported by the National Natural Science Foundation of China (No. 22235006)

摘要: 本研究以吩噻嗪为核心构筑单元,合成了三种五环稠合衍生物E‑2NAPZ‑2NAPPh‑ANT以及两种六环稠合衍生物E‑NAP‑ANT Z‑NAP‑ANT。研究结果表明,在五环体系中,具有不对称结构的 E‑2NAP 在 77 K 溶液中表现出比对称结构的 Z‑2NAP 更强的余辉发射;而 Ph‑ANT 在粉末态下则表现出显著的温度依赖性,其在 293 K 时余辉寿命达到最大值 119.68 ms,该行为主要由热活化延迟荧光机制 (TADF) 主导。当温度超过 293 K 时,TADF 过程与三重态激子的非辐射耗散之间竞争加剧,导致余辉寿命下降。综上,本研究通过调控稠环数量与连接位点,实现了对分子构象、堆积模式及余辉性能的有效调控,为吩噻嗪类余辉材料的设计提供了重要的分子设计思路。

关键词: 吩噻嗪稠环体系, 分子构象, 余辉性能

Abstract:

Based on the phenothiazine core, we have synthesized three pentacyclic derivativesE‑2NAP,Z‑2NAP, andPh‑ANT,together with two hexacyclic derivativesE‑NAP‑ANTandZ‑NAP‑ANT. In the pentacyclic series, the asymmetric derivativeE‑2NAPshows stronger afterglow emission in frozen solution (77 K) than that of the symmetricZ‑2NAP. In the solid state,Ph‑ANTexhibits distinct thermally responsive behavior, with an afterglow lifetime reaching a maximum of 119.68 ms at 293 K, which is primarily attributed to a thermally activated delayed fluorescence (TADF) mechanism. Above 293 K, competition emerges between the TADF pathway and non‑radiative decay channels of triplet excitons, resulting in a reduction in afterglow lifetime. In summary, through rational modulation of the fused‑ring number and substitution positions, this work demonstrates effective adjustment of molecular conformation, solid‑state packing, and room‑temperature afterglow properties, providing important insights for the molecular design of phenothiazine‑based room‑temperature afterglow materials.

Key words: Phenothiazine fused ring, molecular conformation, afterglow properties

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