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Supramolecular chiroptical sensing by achiral AIE-active thiols

文献类型: 外文期刊

作者: Zhang, Xueyan 1 ; Li, Yang 1 ; Wang, Li 2 ; Liu, Hongcheng 2 ;

作者机构: 1.Univ Chinese Acad Sci, Wenzhou Inst, Wenzhou Key Lab Biophys, Wenzhou 325000, Zhejiang, Peoples R China

2.Yunnan Acad Agr Sci, Inst Qual Stand & Testing Technol, Supervis & Testing Ctr Farm Prod Qual, Minist Agr, Kunming 650205, Peoples R China

期刊名称:ORGANIC CHEMISTRY FRONTIERS ( 影响因子:4.7; 五年影响因子:4.5 )

ISSN: 2052-4129

年卷期: 2025 年 12 卷 6 期

页码:

收录情况: SCI

摘要: Rapid and sensitive chiroptical sensing is of great significance for practical applications. Here, a novel rapid supramolecular chiroptical sensing strategy was developed to eliminate possible background interferences and enhance the chiroptical signal by a non-chiral AIE-active thiol click reaction with chiral substrates. These AIE-thiols irreversibly bind amino acids, polypeptides, amines and amino alcohols based on a click-like reaction, and their sensing products further self-assemble, resulting in a higher chiroptical signal output. In particular, the AIE thiol generated from octyloxy-functionalized alpha-cyanostilbene can form supramolecular helix pi-pi stacking in the aggregated state, which can greatly contribute to the chiroptical sensing of the target substrate. The self-assemblies obtained from different AIE thiol sensing reactions exhibit different CD and CPL behaviors due to their different self-assembly modes, which are caused by the subtle differences in the non-covalent C-H & ctdot;pi, [pi & ctdot;pi] and hydrogen bonding interactions of the chiroptical sensing reaction product. Their high reactivity and robust self-assembly sensing mechanism eliminate the interference of chiral substrates and their impurities, improving sensor sensitivity and selectivity. This strategy provides a simple and promising means of detecting chiral molecules, especially those without UV optical activity.

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