| Literature DB >> 32385974 |
Yuanyuan Li1,2, Shunjie Liu1, Huwei Ni3, Haoke Zhang1, Hequn Zhang3,4, Clarence Chuah1, Chao Ma5, Kam Sing Wong5, Jacky W Y Lam1, Ryan T K Kwok1,2, Jun Qian3, Xuefeng Lu6, Ben Zhong Tang1,7,2.
Abstract
The traditional design strategies for highly bright solid-state luminescent materials rely on weakening the intermolecular π-π 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.Entities:
Keywords: ACQ-to-AIE transformation; aggregation-induced emission; cross packing; regioisomerization; two-photon imaging
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Year: 2020 PMID: 32385974 DOI: 10.1002/anie.202005785
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336