Polymerization-Mediated Through-Space Charge Transfer: An Emerging Strategy for Light-Emitting Materials

被引:3
|
作者
Bao, Yinyin [1 ]
机构
[1] Dept Chem & Appl Biosci, ETH Zurich, CH-8093 Zurich, Switzerland
基金
瑞士国家科学基金会;
关键词
ACTIVATED DELAYED FLUORESCENCE; PHOTOINDUCED ELECTRON-TRANSFER; AGGREGATION-INDUCED EMISSION; POLYMERS; RECOMBINATION; DISTANCE; DESIGN; DIODES; DONOR; DNA;
D O I
10.1021/acs.langmuir.3c03376
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Through-space charge transfer (TSCT) has attracted increasing attention owing to its great potential in designing efficient light-emitting molecules and polymers. Complementary to through-bond charge transfer and Fo''rster resonance energy transfer, TSCT offers an alternative approach for the manipulation of molecular fluorescence. Recently, the synergy between TSCT and polymer systems through polymerization-mediated charge transfer has fostered the advancements of innovative light-emitting functional materials featuring thermally activated delayed fluorescence and/or aggregation-induced emission. This perspective highlights the significant progress in tailoring emission properties through structural engineering of donor and acceptor groups within polymeric systems, leveraging the TSCT mechanism. This strategy has transcended the limitations of traditional charge transfer systems with its tolerance to extended donor-acceptor distance, paving the way for novel applications beyond organic light-emitting diodes. The discussion concludes with a forward-looking analysis of potential future research trajectories in the field of polymerization-mediated charge transfer for developing next-generation light-emitting materials.
引用
收藏
页码:3275 / 3282
页数:8
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