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甲醇-水介导的双组装途径在单一组分手性体系中同时制备P螺旋和M螺旋

Simultaneous Fabrication of P and M Helices in One-Component Chiral System by Methanol-Water Mediated Dual Assembly Pathway.

作者信息

Gao Laiben, Yang Kaikai, Xing Chao, Lin Biyan, Zhao Changli, Dou Xiaoqiu, Feng Chuanliang

机构信息

State Key Lab of Metal Matrix Composites, School of Materials Science and Engineering, Shanghai Key Laboratory for Molecular Engineering of Chiral Drugs, Shanghai Jiao Tong University, 800 Dongchuan Road, 200230, Shanghai, P. R. China.

出版信息

Angew Chem Int Ed Engl. 2025 Mar 17;64(12):e202417876. doi: 10.1002/anie.202417876. Epub 2024 Nov 27.

Abstract

The synergetic evolution of multiple chiral structures stemmed from same building units is ubiquitous in nature and vital to living systems, but achieving it in artificial systems remains a challenge. Herein, we report a methanol-water mediated dual assembly pathway strategy for simultaneous construction of P and M helices in one-component chiral system. The conformation of l-phenylaniline derivates (LBpyF) is controlled to folded state in CHOH due to the hydrogen bonds as well as C-H⋅⋅⋅π interaction between LBpyF and CHOH. Addition of HO into above CHOH solution of LBpyF results in the simultaneous occurrence of two self-assembly pathways and double networks of P and M helices were therefore formed, due to the synchronous process of 1) self-assembly of folded LBpyF into M-helices and 2) HO induced unfolding of folded LBpyF molecules followed by self-assembly of them into P-helices. The bipyridine core, phenyl ring, amide unit all adapted into different stacking modes in M-helices and P-helices, and energy analysis indicated that the minority M-helices were more thermodynamically favored products. This study provides an approach to explore synergetic evolution of multiple chiral structures by manipulating the multiple assembly pathway.

摘要

由相同构建单元产生的多种手性结构的协同演化在自然界中普遍存在,对生命系统至关重要,但在人工系统中实现这一点仍然是一个挑战。在此,我们报道了一种甲醇 - 水介导的双组装途径策略,用于在单一组分手性体系中同时构建P螺旋和M螺旋。由于氢键以及L - 苯苯胺衍生物(LBpyF)与CHOH之间的C - H⋅⋅⋅π相互作用,LBpyF的构象在CHOH中被控制为折叠状态。向上述LBpyF的CHOH溶液中加入H₂O会导致两种自组装途径同时发生,因此形成了P螺旋和M螺旋的双网络,这是由于以下同步过程:1)折叠的LBpyF自组装成M螺旋;2)H₂O诱导折叠的LBpyF分子展开,随后它们自组装成P螺旋。联吡啶核心、苯环、酰胺单元在M螺旋和P螺旋中都采用了不同的堆积模式,能量分析表明少数的M螺旋是热力学上更有利的产物。这项研究提供了一种通过操纵多种组装途径来探索多种手性结构协同演化的方法。

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