{"title":"通过甲醇-水介导的双组装途径在单组分手性体系中同时制造 P 和 M 螺旋。","authors":"Laiben Gao, Kaikai Yang, Chao Xing, Biyan Lin, Changli Zhao, Xiaoqiu Dou, Chuan Liang Feng","doi":"10.1002/anie.202417876","DOIUrl":null,"url":null,"abstract":"<p><p>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 CH3OH due to the hydrogen bonds as well as C-H···π interaction between LBpyF and CH3OH. Addition of H2O into above CH3OH 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) H2O 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.</p>","PeriodicalId":125,"journal":{"name":"Angewandte Chemie International Edition","volume":" ","pages":"e202417876"},"PeriodicalIF":16.1000,"publicationDate":"2024-11-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Simultaneous Fabrication of P and M Helices in One-component Chiral System by Methanol-Water Mediated Dual Assembly Pathway.\",\"authors\":\"Laiben Gao, Kaikai Yang, Chao Xing, Biyan Lin, Changli Zhao, Xiaoqiu Dou, Chuan Liang Feng\",\"doi\":\"10.1002/anie.202417876\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>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 CH3OH due to the hydrogen bonds as well as C-H···π interaction between LBpyF and CH3OH. Addition of H2O into above CH3OH 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) H2O 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.</p>\",\"PeriodicalId\":125,\"journal\":{\"name\":\"Angewandte Chemie International Edition\",\"volume\":\" \",\"pages\":\"e202417876\"},\"PeriodicalIF\":16.1000,\"publicationDate\":\"2024-11-19\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Angewandte Chemie International Edition\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://doi.org/10.1002/anie.202417876\",\"RegionNum\":1,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Angewandte Chemie International Edition","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1002/anie.202417876","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
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无处不在,对生命系统至关重要,但在人工系统中实现这一目标仍是一个挑战。在此,我们报告了一种甲醇-水介导的双装配途径策略,可在单组分手性体系中同时构建 P 螺旋和 M 螺旋。由于 LBpyF 和 CH3OH 之间的氢键以及 C-H---π 相互作用,l-苯基苯胺衍生物 (LBpyF) 的构象在 CH3OH 中被控制为折叠状态。在 LBpyF 的上述 CH3OH 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 分子解折,然后自组装成 P 螺旋。双吡啶核心、苯基环、酰胺单元在 M-螺旋和 P-螺旋中都适应了不同的堆叠模式,能量分析表明,少数 M-螺旋是热力学上更有利的产物。这项研究为通过操纵多重组装途径探索多重手性结构的协同演化提供了一种方法。
Simultaneous Fabrication of P and M Helices in One-component Chiral System by Methanol-Water Mediated Dual Assembly Pathway.
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 CH3OH due to the hydrogen bonds as well as C-H···π interaction between LBpyF and CH3OH. Addition of H2O into above CH3OH 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) H2O 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.
期刊介绍:
Angewandte Chemie, a journal of the German Chemical Society (GDCh), maintains a leading position among scholarly journals in general chemistry with an impressive Impact Factor of 16.6 (2022 Journal Citation Reports, Clarivate, 2023). Published weekly in a reader-friendly format, it features new articles almost every day. Established in 1887, Angewandte Chemie is a prominent chemistry journal, offering a dynamic blend of Review-type articles, Highlights, Communications, and Research Articles on a weekly basis, making it unique in the field.