Reversible Photoswitching between Fluorescence and Room Temperature Phosphorescence by Manipulating Excited State Dynamics in Molecular Aggregates

被引:21
|
作者
Wang, Xuanhang [1 ]
Pan, Guocui [1 ]
Ren, Haoxuan [1 ]
Li, Jiashu [1 ]
Xu, Bin [1 ]
Tian, Wenjing [1 ]
机构
[1] Jilin Univ, Coll Chem, State Key Lab Supramol Struct & Mat, Qianjin St 2699, Changchun 130012, Peoples R China
基金
中国国家自然科学基金;
关键词
Fluorescence; Photoswitch; Photochromism; Room temperature phosphorescence; FORSTER ENERGY-TRANSFER;
D O I
10.1002/anie.202114264
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Regulation of fluorescence-phosphorescence pathways in organic molecular aggregate remains a challenge due to the complicated singlet-triplet excited state dynamics process. Herein, we demonstrated a successful example (o-BFT) to realize photoreversible fluorescence and room temperature phosphorescence (RTP) switching based on an effective strategy of integrating a phosphor (dibenzofuran) with a photoswitch (dithienylbenzothiophene). o-BFT exhibited dual emission of fluorescence and RTP in both powder and doping polymer film. Notably, the long-lived RTP of o-BFT could be repeatedly erased and restored through reversible photocyclization and decyclization under alternate ultraviolet and visible photoirradiation. In-depth theoretical and spectroscopic investigations revealed that the triplet inactivation was dominated by a photo-controlled triplet-to-singlet Forster resonance energy transfer from light-activated o-BFT to photoisomer c-BFT. Yet, the initial fluorescence could be preserved in this process to afford a photoreversible fluorescence-RTP switching.
引用
收藏
页数:5
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