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荧光团从“柔性激活”机械发色团的机械化学释放

Mechanochemical Release of Fluorophores from a "Flex-activated" Mechanophore.

作者信息

Yang Fan, Geng Ting, Shen Hang, Kou Yan, Xiao Guanjun, Zou Bo, Chen Yulan

机构信息

State Key Laboratory of Supramolecular Structure and Materials, College of Chemistry, Jilin University, Changchun, 130012, P. R. China.

Fujian Provincial Key Laboratory of Ecology-Toxicological Effects & Control for Emerging Contaminants, Key Laboratory of Ecological Environment and Information Atlas, College of Environmental and Biological Engineering, Putian University, Putian, 351100, P. R. China.

出版信息

Angew Chem Int Ed Engl. 2023 Sep 25;62(39):e202308662. doi: 10.1002/anie.202308662. Epub 2023 Aug 22.

Abstract

Optical force probes that can release force-dependent and visualized signals with minimal changes in the polymer main chains under mechanical load are highly sought after but currently limited. In this study, we introduce a flex-activated mechanophore (FA) based on the Diels-Alder adduct of anthracene and dimethyl acetylenedicarboxylatea that exhibits turn-on mechanofluorescence. We demonstrate that when FA is incorporated into polymer networks or in its crystalline state, it can release fluorescent anthracenes through a retro-Diels-Alder mechanochemical reaction under compression or hydrostatic high pressure, respectively. The flex-activated mechanism of FA is successfully confirmed. Furthermore, we systematically modulate the force delivered to the mechanophore by varying the crosslinking density of the networks and the applied macroscopic pressures. This modulation leads to incremental increases in mechanophore activation, successive release of anthracenes, and quantitative enhancement of fluorescence intensity. The exceptional potential of FA as a sensitive force probe in different bulk states is highlighted, benefiting from its unique flex-activated mode with highly emissive fluorophore releasing. Overall, this report enriches our understanding of the structures and functions of flex-activated mechanophores and polymeric materials.

摘要

在机械负载下能够在聚合物主链变化最小的情况下释放力依赖且可视化信号的光力探针备受追捧,但目前数量有限。在本研究中,我们引入了一种基于蒽与二甲基乙炔二羧酸酯的狄尔斯-阿尔德加合物的挠曲激活机械荧光团(FA),其呈现开启式机械荧光。我们证明,当FA被纳入聚合物网络或以其结晶状态存在时,它可以分别在压缩或静水高压下通过逆狄尔斯-阿尔德机械化学反应释放荧光蒽。FA的挠曲激活机制得到了成功证实。此外,我们通过改变网络的交联密度和施加的宏观压力,系统地调节传递到机械荧光团的力。这种调节导致机械荧光团激活的增量增加、蒽的连续释放以及荧光强度的定量增强。FA作为不同本体状态下灵敏力探针的卓越潜力得以凸显,这得益于其独特的挠曲激活模式以及高发射荧光团的释放。总体而言,本报告丰富了我们对挠曲激活机械荧光团和聚合物材料的结构与功能的理解。

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