Xu Zhuang, Wang Ziming, Zhang Rui, Verma Archana, Neu Justin S, Bairagya Priyotosh, Jeon Sanghyun, Damron Alec M, Rinehart Joshua M, Wagner Justine S, Sabury Sina, Luo Xuyi, Österholm Anna M, Mei Jianguo, Moore Jeffrey S, You Wei, Reynolds John R, Jackson Nicholas E, Diao Ying
Department of Chemical and Biomolecular Engineering, Department of Chemistry, Department of Materials Science and Engineering, Beckman Institute for Advanced Science and Technology, University of Illinois Urbana-Champaign,Urbana, Illinois 61801, United States.
Department of Chemistry, University of North Carolina, Chapel Hill, North Carolina 27599, United States.
J Am Chem Soc. 2025 Sep 17;147(37):33530-33544. doi: 10.1021/jacs.5c07995. Epub 2025 Sep 8.
Spontaneous chiral symmetry breaking remains a fascination in chemistry, biology, materials science, and even astronomy. Chiral symmetry breaking usually requires intrinsic molecular chirality or extrinsic chiral sources but remains rare in nonchiral systems. Here, we reveal a ubiquitous, entropy-driven chiral symmetry breaking mechanism observed in 22 out of 35 conjugated polymers in the absence of any chiral source─a phenomenon overlooked for decades. Chiral assemblies spontaneously occur through liquid-liquid phase separation (LLPS) of lyotropic mesophases from isotropic solutions upon a concentration increase. Machine learning identifies the underpinning molecular features validated by further molecular design. The universality of this phenomenon hints at a possible link between LLPS and chiral symmetry breaking in the origin of life, while paving the way for an emerging frontier of chiral electronics.
自发手性对称性破缺在化学、生物学、材料科学甚至天文学领域一直备受关注。手性对称性破缺通常需要内在分子手性或外在手性源,但在非手性体系中仍然罕见。在此,我们揭示了一种普遍存在的、由熵驱动的手性对称性破缺机制,在35种共轭聚合物中的22种中观察到,且不存在任何手性源——这一现象已被忽视数十年。随着浓度增加,手性聚集体通过各向同性溶液中溶致液晶相的液-液相分离(LLPS)自发形成。机器学习识别出通过进一步分子设计验证的基础分子特征。这一现象的普遍性暗示了在生命起源中LLPS与手性对称性破缺之间可能存在联系,同时为手性电子学这一新兴前沿领域铺平了道路。