Thiophene π-bridge-based second near-infrared luminogens with aggregation-induced emission for biomedical applications

被引:4
|
作者
Tan, Yonghong [1 ]
Sun, Yan [2 ]
Huang, Weigeng [1 ]
Zhu, Dongxia [2 ]
Yan, Dingyuan [1 ,4 ]
Wang, Dong [1 ,4 ]
Tang, Ben Zhong [3 ,5 ]
机构
[1] Shenzhen Univ, Coll Mat Sci & Engn, Ctr AIE Res, Shenzhen, Peoples R China
[2] Northeast Normal Univ, Univ Jilin Prov, Dept Chem, Key Lab Nanobiosensing & Nanobioanalysis, Changchun, Peoples R China
[3] Chinese Univ Hong Kong, Shenzhen Inst Mol Aggregate Sci & Engn, Sch Sci & Engn, Shenzhen, Peoples R China
[4] Shenzhen Univ, Coll Mat Sci & Engn, Ctr AIE Res, Shenzhen 518060, Peoples R China
[5] Chinese Univ Hong Kong, Shenzhen Inst Mol Aggregate Sci & Engn, Sch Sci & Engn, Shenzhen 518172, Peoples R China
关键词
aggregation-induced emission; NIR-II fluorescence imaging; pi-Bridge engineering; FLUORESCENCE;
D O I
10.1002/bio.4606
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
In the past 5 years, aggregation-induced emission luminogens (AIEgens) with emission in the second near-infrared (NIR-II) optical window have aroused great interest in bioimaging and disease phototheranostics, benefiting from the merits of deep penetration depth, reduced light scatting, high spatial resolution, and minimal photodamage. To construct NIR-II AIEgens, thiophene derivatives are frequently adopted as pi-bridge by virtue of their electron-rich feature and good modifiability. Herein, we summarize the recent progress of NIR-II AIEgens by employing thiophene derivatives as pi-bridge mainly compassing unsubstituted thiophene, alkyl thiophene, 3,4-ethylenedioxythiophene, and benzo[c]thiophene, with a discussion on their structure-property relationships and biomedical applications. Finally, a brief conclusion and perspective on this fascinating area are offered.
引用
收藏
页数:11
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