Pamungkas Khurnia Krisna Puji, Yamamoto Riku, Vonesch Maxime, Sakai Naomi, Sagara Yoshimitsu, Matile Stefan
Department of Organic Chemistry, University of Geneva, 1211 Geneva, Switzerland.
National Centre of Competence in Research (NCCR) Molecular Systems Engineering, 4002 Basel, Switzerland.
JACS Au. 2025 Aug 5;5(8):3944-3950. doi: 10.1021/jacsau.5c00579. eCollection 2025 Aug 25.
Fluorescent flippers are twisted push-pull mechanophores that report planarization with red-shifted absorption and an increase in fluorescence intensity and lifetime. Until today, their planarization by physical forces has focused on compression to visualize physical forces in biology. Here, we show that planarization can also be achieved by stretching of flipper probes that are equipped with tethers in their core and to visualize mechanical stress in polymeric materials. The synthesis of dithieno-[3,2-:2',3'-]-thiophene dimers with alcohols extending from their twisted core is accomplished in 17 steps. Covalently integrated into polyurethanes, these core-substituted flippers exhibit an excitation-wavelength-dependent fluorescence enhancement upon polymer stretching, validating their mode of action. Noncovalently interfaced flipper controls are much less responsive. In light of the importance their fluorogenic compression has reached in biology, synthetic access to flippers that can be stretched rather than compressed and use in materials rather than life sciences opens up significant, fundamentally new perspectives for flipper research.
荧光翻转体是扭曲的推挽式机械力发色团,通过红移吸收以及荧光强度和寿命的增加来报告平面化。直到如今,它们通过物理力实现的平面化一直聚焦于压缩,以可视化生物学中的物理力。在此,我们表明,对于在其核心配备系链的翻转体探针,通过拉伸也可实现平面化,从而可视化聚合物材料中的机械应力。从其扭曲核心延伸出醇基的二噻吩并-[3,2-:2',3'-]噻吩二聚体的合成需17步完成。这些核心取代的翻转体共价整合到聚氨酯中后,在聚合物拉伸时表现出与激发波长相关的荧光增强,验证了其作用模式。非共价连接的翻转体对照的响应则要小得多。鉴于其荧光压缩在生物学中已具有的重要性,合成可拉伸而非压缩且用于材料而非生命科学的翻转体,为翻转体研究开辟了重要的、全新的基本视角。