磷光
材料科学
系统间交叉
荧光
光化学
发色团
光致发光
接受者
超分子化学
激子
光电子学
分子
单重态
激发态
有机化学
化学
原子物理学
量子力学
物理
凝聚态物理
作者
Zecong Ye,Mingbing Lian,Zhiyao Yang,Yu Fu,Zhenwen Wang,Yingxiao Mu,Shaomin Ji,Hao‐Li Zhang,Lihua Yuan,Zhenguo Chi,Yanping Huo
标识
DOI:10.1002/adom.202202521
摘要
Abstract Despite vast applications of macrocycles in supramolecular chemistry, achieving long‐lived emissions including room‐temperature phosphorescence (RTP) or thermally activated delayed fluorescence (TADF) for potential use still presents a great challenge. This work first reports hydrogen‐bonded (H‐bonded) macrocycles emitting RTP and TADF by introducing various donors onto the same aramide skeleton containing a rigid acceptor. The formation of charge transfer effectively enhances the photoluminescence efficiency. Aromatic carbonyl groups promote the intersystem crossing. The drastically reduced flexibility of chromophores fixed by the H‐bonded macrocyclic framework contributes to suppress the nonradiative decay to stabilize triplet excitons. Therefore, RTP and TADF are acquired by altering donors, and are systematically revealed by comparisons with control compounds and theoretical calculations. Finally, near white‐light emission (CIE, 0.30, 0.33) is realized via host–guest interactions.
科研通智能强力驱动
Strongly Powered by AbleSci AI