Aikaterini Mathianaki, Aysha Demeler, Adrian Dömling, Federico Ferrrari, Frieda Clara M. Scheelje, Hilke Bahmann, Guillaume Delaittre
{"title":"Towards the Synthesis of Polythiazolines: A Post-polymerization Approach","authors":"Aikaterini Mathianaki, Aysha Demeler, Adrian Dömling, Federico Ferrrari, Frieda Clara M. Scheelje, Hilke Bahmann, Guillaume Delaittre","doi":"10.1039/d4py00930d","DOIUrl":null,"url":null,"abstract":"The synthesis of novel tertiary polythioamide copolymers, analogues of poly(2-ethyl-2-oxazoline) (PEtOx), is reported. Firstly, the direct synthesis of poly(2-methyl-2-thiazoline) was attempted via the cationic ring-opening polymerization of 2-methyl-2-thiazoline, in analogy to the well-known 2-alkyl-2-oxazoline monomers. Since no conversion was monitored under several conditions – which was investigated in parallel by density functional theory calculations – the post-polymerization modification of PEtOx using the Lawesson’s reagent was successfully utilized, yielding poly(2-ethyl-2-thiazoline)-<em>co</em>-(2-ethyl-2-oxazoline) copolymers with up to 95 mol% of the thioamide unit. The newly synthesized copolymers exhibited significantly lower water solubility and thermal stability than the pristine PEtOx, as demonstrated during cloud point temperature determination and thermal gravimetric analysis respectively. Moreover, the glass transition temperature of the copolymers increases linearly with increasing oxygen-thiol exchange.","PeriodicalId":100,"journal":{"name":"Polymer Chemistry","volume":"37 1","pages":""},"PeriodicalIF":4.1000,"publicationDate":"2024-12-05","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/d4py00930d","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
The synthesis of novel tertiary polythioamide copolymers, analogues of poly(2-ethyl-2-oxazoline) (PEtOx), is reported. Firstly, the direct synthesis of poly(2-methyl-2-thiazoline) was attempted via the cationic ring-opening polymerization of 2-methyl-2-thiazoline, in analogy to the well-known 2-alkyl-2-oxazoline monomers. Since no conversion was monitored under several conditions – which was investigated in parallel by density functional theory calculations – the post-polymerization modification of PEtOx using the Lawesson’s reagent was successfully utilized, yielding poly(2-ethyl-2-thiazoline)-co-(2-ethyl-2-oxazoline) copolymers with up to 95 mol% of the thioamide unit. The newly synthesized copolymers exhibited significantly lower water solubility and thermal stability than the pristine PEtOx, as demonstrated during cloud point temperature determination and thermal gravimetric analysis respectively. Moreover, the glass transition temperature of the copolymers increases linearly with increasing oxygen-thiol exchange.
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.