{"title":"可变形液滴约束下手性物质的受控扭动","authors":"Rongjuan Liu, Xiaobin Dai, Benyou Li, Qiang Li, Jingjing Wei*, Li-Tang Yan* and Zhijie Yang*, ","doi":"10.1021/jacs.5c05428","DOIUrl":null,"url":null,"abstract":"<p >Chirality─the property of being nonsuperimposable on its mirror image─plays a fundamental role in shaping how materials interact with light, molecules, and external fields. This property is key to advancements in areas such as quantum computing, flexible electronics, and smart sensors. However, controlling chirality in materials beyond the molecular scale has remained a significant challenge. In this study, we demonstrate a new approach for controlling the chirality of self-assembled materials by manipulating their behavior within deformable emulsion droplets. These droplets, ranging from nanometers to micrometers in size, guide the twisting of chiral fibrils formed through molecular self-assembly, with the droplet size determining the chirality. Our results, based on over 20 different chiral molecules, show that droplet confinement can induce chirality inversion, where nanoscale and microscale droplets exhibit opposite handedness. When the size of the droplet matches the persistence length of the chiral fibrils, the particles form superhelical structures. If mismatched, the fibrils twist in the opposite direction. In addition, we show that surfactant-coated helical fibrils can elongate into micrometer-long structures via living self-assembly, with chirality dictated by the as-formed helical fibrils and not the additional monomers. This work paves the way for new strategies to design and control chiral materials with tailored properties for a range of cutting-edge applications.</p>","PeriodicalId":49,"journal":{"name":"Journal of the American Chemical Society","volume":"147 26","pages":"22901–22910"},"PeriodicalIF":15.6000,"publicationDate":"2025-06-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Controlled Writhing of Chiral Matter in Deformable Droplet Confinement\",\"authors\":\"Rongjuan Liu, Xiaobin Dai, Benyou Li, Qiang Li, Jingjing Wei*, Li-Tang Yan* and Zhijie Yang*, \",\"doi\":\"10.1021/jacs.5c05428\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >Chirality─the property of being nonsuperimposable on its mirror image─plays a fundamental role in shaping how materials interact with light, molecules, and external fields. This property is key to advancements in areas such as quantum computing, flexible electronics, and smart sensors. However, controlling chirality in materials beyond the molecular scale has remained a significant challenge. In this study, we demonstrate a new approach for controlling the chirality of self-assembled materials by manipulating their behavior within deformable emulsion droplets. These droplets, ranging from nanometers to micrometers in size, guide the twisting of chiral fibrils formed through molecular self-assembly, with the droplet size determining the chirality. Our results, based on over 20 different chiral molecules, show that droplet confinement can induce chirality inversion, where nanoscale and microscale droplets exhibit opposite handedness. When the size of the droplet matches the persistence length of the chiral fibrils, the particles form superhelical structures. If mismatched, the fibrils twist in the opposite direction. In addition, we show that surfactant-coated helical fibrils can elongate into micrometer-long structures via living self-assembly, with chirality dictated by the as-formed helical fibrils and not the additional monomers. This work paves the way for new strategies to design and control chiral materials with tailored properties for a range of cutting-edge applications.</p>\",\"PeriodicalId\":49,\"journal\":{\"name\":\"Journal of the American Chemical Society\",\"volume\":\"147 26\",\"pages\":\"22901–22910\"},\"PeriodicalIF\":15.6000,\"publicationDate\":\"2025-06-16\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of the American Chemical Society\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://pubs.acs.org/doi/10.1021/jacs.5c05428\",\"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":"Journal of the American Chemical Society","FirstCategoryId":"92","ListUrlMain":"https://pubs.acs.org/doi/10.1021/jacs.5c05428","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
Controlled Writhing of Chiral Matter in Deformable Droplet Confinement
Chirality─the property of being nonsuperimposable on its mirror image─plays a fundamental role in shaping how materials interact with light, molecules, and external fields. This property is key to advancements in areas such as quantum computing, flexible electronics, and smart sensors. However, controlling chirality in materials beyond the molecular scale has remained a significant challenge. In this study, we demonstrate a new approach for controlling the chirality of self-assembled materials by manipulating their behavior within deformable emulsion droplets. These droplets, ranging from nanometers to micrometers in size, guide the twisting of chiral fibrils formed through molecular self-assembly, with the droplet size determining the chirality. Our results, based on over 20 different chiral molecules, show that droplet confinement can induce chirality inversion, where nanoscale and microscale droplets exhibit opposite handedness. When the size of the droplet matches the persistence length of the chiral fibrils, the particles form superhelical structures. If mismatched, the fibrils twist in the opposite direction. In addition, we show that surfactant-coated helical fibrils can elongate into micrometer-long structures via living self-assembly, with chirality dictated by the as-formed helical fibrils and not the additional monomers. This work paves the way for new strategies to design and control chiral materials with tailored properties for a range of cutting-edge applications.
期刊介绍:
The flagship journal of the American Chemical Society, known as the Journal of the American Chemical Society (JACS), has been a prestigious publication since its establishment in 1879. It holds a preeminent position in the field of chemistry and related interdisciplinary sciences. JACS is committed to disseminating cutting-edge research papers, covering a wide range of topics, and encompasses approximately 19,000 pages of Articles, Communications, and Perspectives annually. With a weekly publication frequency, JACS plays a vital role in advancing the field of chemistry by providing essential research.