Kuan Chen, Binhao Li, Chuanhao Liu, Yanju Luo, Kaixin Yu, Mengjiao Jia, Yan Huang, Zhiyun Lu
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引用次数: 0
Abstract
The realization of long‐lived charge‐transfer‐based organic room‐temperature phosphorescence (3CT‐RTP, τPh = 210 ms) via the construction of U‐shaped donor–acceptor (D–A) dyads is impeded by suboptimal phosphorescence efficiency ( = 6%). Herein, we reveal that modifying the skeleton of D–A dyads from U‐shaped to V‐shaped configurations yields 3CT‐RTP with both long τPh (150–220 ms) and high (13%–25%). This improvement stems from preserving a substantial degree of forbiddenness in the radiative transition process of the compound while simultaneously increasing its D–A dihedral angle, which can promote more efficient spin‐orbit coupling and thus more rapid intersystem crossing. Additionally, augmenting the framework rigidity of a V‐shaped D–A dyad can potentially reduce the non‐radiative transition rate constant of triplet excitons (knr,T), thereby facilitating the attainment of long τPh and high .
期刊介绍:
Angewandte Chemie, a journal of the German Chemical Society (GDCh), maintains a leading position among scholarly journals in general chemistry with an impressive Impact Factor of 16.6 (2022 Journal Citation Reports, Clarivate, 2023). Published weekly in a reader-friendly format, it features new articles almost every day. Established in 1887, Angewandte Chemie is a prominent chemistry journal, offering a dynamic blend of Review-type articles, Highlights, Communications, and Research Articles on a weekly basis, making it unique in the field.