State Key Laboratory of Analytical Chemistry for Life Science, Jiangsu Key Laboratory of Advanced Organic Materials, School of Chemistry and Chemical Engineering, Nanjing University, 210023, Nanjing, China.
Ma'anShan High-Tech Research Institute of Nanjing University, Ma'anShan, 238200, China.
Nat Commun. 2023 Feb 3;14(1):590. doi: 10.1038/s41467-023-36131-w.
Controlling molecular motion is one of hot topics in the field of chemistry. Molecular rotors have wide applications in building nanomachines and functional materials, due to their controllable rotations. Hence, the development of novel rotor systems, controlled by external stimuli, is desirable. Pillar[n]arenes, a class of macrocycles, have a unique planar chirality, in which two stable conformational isomers pR and pS would interconvert by oxygen-through-the-annulus rotations of their hydroquinone rings. We observe the differential kinetic traits of planar chirality transformation in sodium carboxylate pillar[5]arene (WP5-Na) and ammonium carboxylate pillar[5]arene (WP5-NH), which inspire us to construct a promising rotary platform in anionic pillar[5]arenes (WP5) skeletons. Herein, we demonstrate the non-negligible effect of counter cations on rotational barriers of hydroquinone rings in WP5, which enables a cation grease/brake rotor system. Applications of this tunable rotor system as fluorescence switch and anti-counterfeiting ink are further explored.
控制分子运动是化学领域的热门话题之一。由于分子转子的旋转可控性,它们在构建纳米机器和功能材料方面有广泛的应用。因此,开发受外部刺激控制的新型转子系统是可取的。[n]柱芳烃是一类大环化合物,具有独特的平面手性,其中两个稳定的构象异构体 pR 和 pS 通过其对苯二酚环的氧通过环旋转相互转化。我们观察到羧酸钠柱[5]芳烃(WP5-Na)和铵羧酸钠柱[5]芳烃(WP5-NH)中平面手性转变的差异动力学特征,这启发我们在阴离子柱[5]芳烃(WP5)骨架中构建一个有前途的旋转平台。在此,我们证明了抗衡阳离子对 WP5 中对苯二酚环旋转势垒的不可忽视的影响,这使得阳离子脂/刹车转子系统成为可能。进一步探索了这种可调转子系统作为荧光开关和防伪油墨的应用。