{"title":"通用可见光光增塑剂聚合","authors":"Shuangqi Lian, Steven P. Armes, Zesheng An","doi":"10.31635/ccschem.024.202404894","DOIUrl":null,"url":null,"abstract":"<p>Currently, there is no versatile method for the synthesis of high molecular weight (MW) polymers by controlled radical polymerization from a broad range of monomers using a single agent. Herein, we report a universal photoiniferter reversible addition-fragmentation chain transfer (RAFT) polymerization formulation using a suitable pyrazole-based chain transfer agent (CTA) combined with blue light irradiation. Well-controlled polymerization was observed for methyl methacrylate (MMA), methyl acrylate (MA), <i>N</i>,<i>N</i>-dimethylacrylamide (DMA), and <i>N</i>-vinylpyrrolidone (NVP). High polymerization rates were achieved, attributed to the high molar absorption coefficient of the pyrazole-based CTA and its rapid rate of photolysis. Poly(methyl acrylate) (PMA) and poly(<i>N</i>,<i>N</i>-dimethylacrylamide) (PDMA) syntheses yielded low-dispersity ultrahigh MW chains (>10<sup>6</sup> g mol<sup>−1</sup>, <i>Ð</i> < 1.3). High end-group fidelity enabled the preparation of well-defined high MW diblock copolymers comprising both more activated and less activated monomers, including PDMA-<i>b</i>-PNVP and PMA-<i>b</i>-PNVP. Such syntheses demonstrated that visible light-mediated photoiniferter RAFT polymerization conducted using pyrazole-based CTAs was both highly efficient and versatile.</p>","PeriodicalId":9810,"journal":{"name":"CCS Chemistry","volume":"6 1","pages":""},"PeriodicalIF":9.4000,"publicationDate":"2024-10-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Universal Visible-Light Photoiniferter Polymerization\",\"authors\":\"Shuangqi Lian, Steven P. Armes, Zesheng An\",\"doi\":\"10.31635/ccschem.024.202404894\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>Currently, there is no versatile method for the synthesis of high molecular weight (MW) polymers by controlled radical polymerization from a broad range of monomers using a single agent. Herein, we report a universal photoiniferter reversible addition-fragmentation chain transfer (RAFT) polymerization formulation using a suitable pyrazole-based chain transfer agent (CTA) combined with blue light irradiation. Well-controlled polymerization was observed for methyl methacrylate (MMA), methyl acrylate (MA), <i>N</i>,<i>N</i>-dimethylacrylamide (DMA), and <i>N</i>-vinylpyrrolidone (NVP). High polymerization rates were achieved, attributed to the high molar absorption coefficient of the pyrazole-based CTA and its rapid rate of photolysis. Poly(methyl acrylate) (PMA) and poly(<i>N</i>,<i>N</i>-dimethylacrylamide) (PDMA) syntheses yielded low-dispersity ultrahigh MW chains (>10<sup>6</sup> g mol<sup>−1</sup>, <i>Ð</i> < 1.3). High end-group fidelity enabled the preparation of well-defined high MW diblock copolymers comprising both more activated and less activated monomers, including PDMA-<i>b</i>-PNVP and PMA-<i>b</i>-PNVP. Such syntheses demonstrated that visible light-mediated photoiniferter RAFT polymerization conducted using pyrazole-based CTAs was both highly efficient and versatile.</p>\",\"PeriodicalId\":9810,\"journal\":{\"name\":\"CCS Chemistry\",\"volume\":\"6 1\",\"pages\":\"\"},\"PeriodicalIF\":9.4000,\"publicationDate\":\"2024-10-30\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"CCS Chemistry\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.31635/ccschem.024.202404894\",\"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":"CCS Chemistry","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.31635/ccschem.024.202404894","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
Currently, there is no versatile method for the synthesis of high molecular weight (MW) polymers by controlled radical polymerization from a broad range of monomers using a single agent. Herein, we report a universal photoiniferter reversible addition-fragmentation chain transfer (RAFT) polymerization formulation using a suitable pyrazole-based chain transfer agent (CTA) combined with blue light irradiation. Well-controlled polymerization was observed for methyl methacrylate (MMA), methyl acrylate (MA), N,N-dimethylacrylamide (DMA), and N-vinylpyrrolidone (NVP). High polymerization rates were achieved, attributed to the high molar absorption coefficient of the pyrazole-based CTA and its rapid rate of photolysis. Poly(methyl acrylate) (PMA) and poly(N,N-dimethylacrylamide) (PDMA) syntheses yielded low-dispersity ultrahigh MW chains (>106 g mol−1, Ð < 1.3). High end-group fidelity enabled the preparation of well-defined high MW diblock copolymers comprising both more activated and less activated monomers, including PDMA-b-PNVP and PMA-b-PNVP. Such syntheses demonstrated that visible light-mediated photoiniferter RAFT polymerization conducted using pyrazole-based CTAs was both highly efficient and versatile.
期刊介绍:
CCS Chemistry, the flagship publication of the Chinese Chemical Society, stands as a leading international chemistry journal based in China. With a commitment to global outreach in both contributions and readership, the journal operates on a fully Open Access model, eliminating subscription fees for contributing authors. Issued monthly, all articles are published online promptly upon reaching final publishable form. Additionally, authors have the option to expedite the posting process through Immediate Online Accepted Article posting, making a PDF of their accepted article available online upon journal acceptance.