{"title":"Large Aromatic Amide Helices via Living Polycondensation","authors":"Dinh Phuong Trinh Nguyen, Saquib Farooq, Nicoleta Meyer, Andreas F.M. Kilbinger","doi":"10.1039/d5py00275c","DOIUrl":null,"url":null,"abstract":"We employ a living polymerization strategy and a crescent-shaped monomer to synthesize large aromatic amide helices with cavity sizes exceeding 1 nm. These polymeric foldamer helices are stabilized by a continuous strand of three-center hydrogen bonds, ensuring structural integrity. Our method efficiently yields polymeric helices of varying lengths while also producing macrocycles as side products when targeting higher molecular weights. The isolation and characterization of a 7-mer macrocycle provided key insights into the number of repeat units required to complete a full turn of the corresponding polymeric helix. Additionally, macrocycles were obtained in greater quantities by performing the polycondensation in the absence of an initiator. This straightforward and versatile approach paves the way for the development of novel materials with potential applications in host-guest chemistry, catalysis, and molecular transport.","PeriodicalId":100,"journal":{"name":"Polymer Chemistry","volume":"70 1","pages":""},"PeriodicalIF":4.1000,"publicationDate":"2025-05-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Polymer Chemistry","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1039/d5py00275c","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"POLYMER SCIENCE","Score":null,"Total":0}
引用次数: 0
Abstract
We employ a living polymerization strategy and a crescent-shaped monomer to synthesize large aromatic amide helices with cavity sizes exceeding 1 nm. These polymeric foldamer helices are stabilized by a continuous strand of three-center hydrogen bonds, ensuring structural integrity. Our method efficiently yields polymeric helices of varying lengths while also producing macrocycles as side products when targeting higher molecular weights. The isolation and characterization of a 7-mer macrocycle provided key insights into the number of repeat units required to complete a full turn of the corresponding polymeric helix. Additionally, macrocycles were obtained in greater quantities by performing the polycondensation in the absence of an initiator. This straightforward and versatile approach paves the way for the development of novel materials with potential applications in host-guest chemistry, catalysis, and molecular transport.
期刊介绍:
Polymer Chemistry welcomes submissions in all areas of polymer science that have a strong focus on macromolecular chemistry. Manuscripts may cover a broad range of fields, yet no direct application focus is required.