分子内力
分子间力
氢键
超分子化学
聚集诱导发射
结构异构体
接受者
荧光
组合化学
化学
立体化学
有机化学
分子
凝聚态物理
量子力学
物理
作者
Ziwei Xu,Bingling Zhang,Shusen Chen,Xudong Zou,Yanhong Lin,Chenxing Gong,Xiong Yin,Tony D. James,Xiao‐Le Zhou,Leyu Wang
出处
期刊:Small
[Wiley]
日期:2024-08-13
卷期号:20 (47)
被引量:4
标识
DOI:10.1002/smll.202403071
摘要
Abstract Regio‐isomers are utilized to design innovative AIE luminogens (AIEgens) by regulating molecular aggregation behavior. However, relevant examples are limited, and the underlying mechanism is not fully understood. Herein, a regio‐isomer strategy is used to develop AIEgens by precisely regulating the intermolecular interactions in the solid state. Among the regio‐isomers it is investigated, ortho‐ isomer ( DCM‐O3‐O7 ) exhibits enhanced AIE‐activity than the para ‐ isomer ( DCM‐P6 ), and the size of the ortho ‐ substituents is crucial for the AIE performance. The underlying mechanism of the strategy is revealed using DFT calculations and single‐crystal analysis. Dual hydrogen bonds (C─H∙∙∙π and C─H∙∙∙N) are generated between the molecules, which contributes to form dimers, tetramers, and 1D supramolecular structures in the crystal. By restricting intramolecular motion and attenuating π – π interactions, solid‐state fluorescence is significantly enhanced. This strategy's effectiveness is validated using other donor–acceptor fluorophores, with DCM‐O6 and its analogues serving as efficient probes for bioimaging applications. Notably, DCM‐OM , which bears a morpholinyl instead of piperidinyl group, displayed strong lysosome‐targeting ability and photostability; DCM‐OP , incorporated by the hydrophilic quaternary ammonium group, exhibited wash‐free imaging and cell membrane‐targeting capabilities; and DCM‐O6 nanoparticles enabled high‐fidelity in vivo tumor imaging. Therefore, this strategy affords a general method for designing bright AIEgens.
科研通智能强力驱动
Strongly Powered by AbleSci AI