Regulation of excitation transit ons by molecular design endowing full-color-tunable emissions with unexpected high quantum yields for bioimaging application
Regulation of excitation transit ons by molecular design endowing full-color-tunable emissions with unexpected high quantum yields for bioimaging application作者机构:Beijing National Laboratory for Molecular SciencesCAS Key Laboratory of Organic SolidsInstitute of ChemistryChinese Academy of SciencesBeijing 100190China University of Chinese Academy of SciencesBeijing 100049China
出 版 物:《Science China Chemistry》 (中国科学(化学英文版))
年 卷 期:2018年第61卷第4期
页 面:418-426页
核心收录:
学科分类:081702[工学-化学工艺] 08[工学] 0817[工学-化学工程与技术]
基 金:supported by the National Basic Research Program of China(2014CB643502) the Strategic Priority Research Program of the Chinese Academy of Sciences(XDB12010200) the National Natural Science Foundation of China(91333113,21572234)
主 题:donor-aeceptors systems dyes thieno[3 4-b]thiophene fluorescence bioimaging
摘 要:Organic fluorophores are indispensible in chemical/biological imaging. The conjugated fluorescent molecules simultaneously possessing highly tunable emission, high quantum yield in solvents of different polarities, and large Stokes shift are quite rare. Herein, we report a new category of fluorophores based on diarylated thieno[3,4-b]thiophenes efficiently synthesized by direct C-H arylation reaction. TbT-Fluors showed full-color-tunable emissions with large Stokes shifts. Intriguingly,the fluorescence quantum yields of TbT-Fluors are barely sensitive to solvent polarities, approaching 100%. Based on photophysical and theoretical investigations, we found that the enhanced oscillator strength of the S_1-S_0 transition and increased T2-S1 energy difference can sufficiently compensate the negative effect from the decreased energy gap and increased reorganization energy in dimethyl sulfoxide(DMSO). Bioimaging applications revealed that some TbT-Fluors can penetrate the cell membrane and are superior for imaging in terms of high photochemical stability and low cytotoxicity. Furthermore, TbT-PhF exhibits specific colocalization with mitochondria in living cells.