Li Jingjing, Yin Fang, Wang Jianhong, Du Huachuan, Xu Fan, Meskers Stefan, Li Yudong, Wijker Stefan, Peng Yu, Bellan Riccardo, Vantomme Ghislaine, Song Jian, Liu Chun-Sen, Meijer E W
College of New Energy, Zhengzhou University of Light Industry, Zhengzhou 450002, China.
Institute for Complex Molecular Systems and Laboratory of Macromolecular and Organic Chemistry, Eindhoven University of Technology, Eindhoven 5600 MB, Netherlands.
J Am Chem Soc. 2025 May 21;147(20):17361-17371. doi: 10.1021/jacs.5c03844. Epub 2025 May 9.
This study reports a supramolecular gel system capable of dynamic gel-to-gel transformations and reversible inversion of optical activity between superhelical and single-helical structures without passing through a sol phase. Inspired by collagen-like adaptability, the system utilizes 4-pyridinylboronic acid and guanosine as building blocks. Hierarchical assembly is achieved through pH-responsive boronic ester formation and guanosine-mediated G-quadruplex stacking, enabling transitions between superhelices and single helices with opposite optical activity. The system employs three regulatory pathways: bidirectional pH modulation, monotonic pH increase, and monotonic pH decrease, demonstrating programmable and reversible control over chirality, morphology, and mechanical properties. In the autonomous pH regulation, we have created an out-of-equilibrium hydrogel system with controlled switching of optical activity. Unlike traditional gel-sol-gel systems, this gel maintains macroscopic stability during transformations. Our remarkable finding bridges the gap between static supramolecular assemblies and dynamic soft materials, offering a platform for designing functional, biomimetic systems. The combination of hierarchical organization, dynamic chirality control, and robust programmability positions this gel for applications in adaptive optics, responsive biomaterials, and programmable soft matter.
本研究报道了一种超分子凝胶体系,该体系能够进行动态的凝胶-凝胶转变,以及在超螺旋结构和单螺旋结构之间进行光学活性的可逆反转,且无需经过溶胶相。受类胶原适应性的启发,该体系利用4-吡啶硼酸和鸟苷作为构建模块。通过pH响应性硼酸酯的形成和鸟苷介导的G-四链体堆积实现分级组装,从而实现具有相反光学活性的超螺旋和单螺旋之间的转变。该体系采用三种调节途径:双向pH调节、pH单调升高和pH单调降低,展示了对手性、形态和机械性能的可编程和可逆控制。在自主pH调节中,我们创建了一个具有可控光学活性切换的非平衡水凝胶体系。与传统的凝胶-溶胶-凝胶体系不同,这种凝胶在转变过程中保持宏观稳定性。我们这一显著发现弥合了静态超分子组装体与动态软材料之间的差距,为设计功能性仿生体系提供了一个平台。分级组织、动态手性控制和强大的可编程性相结合,使这种凝胶可应用于自适应光学、响应性生物材料和可编程软物质领域。