TY - JOUR
T1 - Self-Regulating Hydrogel with Reversible Optical Activity in Its Gel-to-Gel Transformation
AU - Li, Jingjing
AU - Yin, Fang
AU - Wang, Jianhong
AU - Du, Huachuan
AU - Xu, Fan
AU - Meskers, Stefan
AU - Li, Yudong
AU - Wijker, Stefan
AU - Peng, Yu
AU - Bellan, Riccardo
AU - Vantomme, Ghislaine
AU - Song, Jian
AU - Liu, Chun Sen
AU - Meijer, E. W.
PY - 2025/5/21
Y1 - 2025/5/21
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=105004675342&partnerID=8YFLogxK
U2 - 10.1021/jacs.5c03844
DO - 10.1021/jacs.5c03844
M3 - Article
C2 - 40344185
AN - SCOPUS:105004675342
SN - 0002-7863
VL - 147
SP - 17361
EP - 17371
JO - Journal of the American Chemical Society
JF - Journal of the American Chemical Society
IS - 20
ER -