ACQ-to-AIE Transformation: Tuning Molecular Packing by Regioisomerization for Two-Photon NIR Bioimaging

被引:163
作者
Li, Yuanyuan [1 ,7 ]
Liu, Shunjie [1 ]
Ni, Huwei [3 ]
Zhang, Haoke [1 ]
Zhang, Hequn [3 ,4 ]
Chuah, Clarence [1 ]
Ma, Chao [5 ]
Wong, Kam Sing [5 ]
Lam, Jacky W. Y. [1 ]
Kwok, Ryan T. K. [1 ,7 ]
Qian, Jun [3 ]
Lu, Xuefeng [2 ]
Tang, Ben Zhong [1 ,6 ,7 ]
机构
[1] Hong Kong Univ Sci & Technol, Chinese Natl Engn Res Ctr Tissue Restorat & Recon, Dept Chem,Hong Kong Branch,Inst Adv Study, State Key Lab Mol Neurosci,Dept Chem & Biol Engn, Clear Water Bay, Hong Kong, Peoples R China
[2] Fudan Univ, Dept Mat Sci, Shanghai 200438, Peoples R China
[3] Zhejiang Univ, Coll Opt Sci & Engn, State Key Lab Modern Opt Instrumentat, Ctr Opt & Electromagnet Res, Hangzhou 310058, Peoples R China
[4] Zhejiang Univ, Sch Med, Affiliated Hosp 2, Interdisciplinary Inst Neurosci & Technol ZIINT, Hangzhou 310020, Peoples R China
[5] Hong Kong Univ Sci & Technol, Dept Phys, Kowloon, Clear Water Bay, Hong Kong, Peoples R China
[6] South China Univ Technol, Ctr Aggregat Induced Emiss, SCUT HKUST Joint Res Inst, State Key Lab Luminescent Mat & Devices, Guangzhou 510640, Peoples R China
[7] HKUST Shenzhen Res Inst, 9 Yuexing 1st RD,Hitech Pk, Shenzhen 518057, Peoples R China
基金
美国国家科学基金会; 中国国家自然科学基金;
关键词
ACQ-to-AIE transformation; aggregation-induced emission; cross packing; regioisomerization; two-photon imaging; AGGREGATION-INDUCED EMISSION; INTRAMOLECULAR CHARGE-TRANSFER; SOLID-STATE FLUORESCENCE; ABSORPTION; RED; STRATEGIES; DESIGN; PROBE;
D O I
10.1002/anie.202005785
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The traditional design strategies for highly bright solid-state luminescent materials rely on weakening the intermolecular pi-pi interactions, which may limit diversity when developing new materials. Herein, we propose a strategy of tuning the molecular packing mode by regioisomerization to regulate the solid-state fluorescence. TBP-e-TPA with a molecular rotor in the end position of a planar core adopts a long-range cofacial packing mode, which in the solid state is almost non-emissive. By shifting molecular rotors to the bay position, the resultant TBP-b-TPA possesses a discrete cross packing mode, giving a quantum yield of 15.6 +/- 0.2 %. These results demonstrate the relationship between the solid-state fluorescence efficiency and the molecule's packing mode. Thanks to the good photophysical properties, TBP-b-TPA nanoparticles were used for two-photon deep brain imaging. This molecular design philosophy provides a new way of designing highly bright solid-state fluorophores.
引用
收藏
页码:12822 / 12826
页数:5
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