Ihor M. Tkachenko, Yuriy I. Kurioz, Ruslan M. Kravchuk, Alexander L. Tolstov, Anatoliy V. Glushchenko, Vassili G. Nazarenko and Valery V. Shevchenko
{"title":"开发聚合物主链中含有偶氮苯基团的光响应型含氟聚(芳基醚)共聚物†。","authors":"Ihor M. Tkachenko, Yuriy I. Kurioz, Ruslan M. Kravchuk, Alexander L. Tolstov, Anatoliy V. Glushchenko, Vassili G. Nazarenko and Valery V. Shevchenko","doi":"10.1039/D3ME00150D","DOIUrl":null,"url":null,"abstract":"<p >A novel light-responsive poly(arylene ether) copolymer with both azobenzene and perfluorinated biphenylene units as well as <em>meta</em>-linked fragments in the main polymer chain is synthesized. The copolymer is synthesized using aromatic nucleophilic substitution reaction from decafluorobiphenyl and two dihydroxyl-substituted monomers, fluorinated bis-azobenzene-based phenol derivative, and resorcinol. The chemical structure of the copolymer is characterized using <small><sup>1</sup></small>H, <small><sup>19</sup></small>F NMR, FTIR, Raman and UV/vis spectroscopy techniques. The polymer shows remarkable solubility in organic solvents resulting in the formation of robust, self-supporting films. It displays impressive mechanical characteristics as well as remarkable resistance to thermo-oxidative degradation. Under UV light irradiation, photoisomerization occurs both in solution and in the solid copolymer film. The solid polymer films exhibit intense and stable birefringence changes upon the irradiation, enabling the fabrication of diffraction gratings. The study indicates that this synthetic approach is a simple and effective method for designing light-responsive materials.</p>","PeriodicalId":91,"journal":{"name":"Molecular Systems Design & Engineering","volume":" 2","pages":" 149-157"},"PeriodicalIF":3.2000,"publicationDate":"2023-11-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Development of a light-responsive fluorinated poly(arylene ether) copolymer containing azobenzene groups in the main polymer chain†\",\"authors\":\"Ihor M. Tkachenko, Yuriy I. Kurioz, Ruslan M. Kravchuk, Alexander L. Tolstov, Anatoliy V. Glushchenko, Vassili G. Nazarenko and Valery V. Shevchenko\",\"doi\":\"10.1039/D3ME00150D\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >A novel light-responsive poly(arylene ether) copolymer with both azobenzene and perfluorinated biphenylene units as well as <em>meta</em>-linked fragments in the main polymer chain is synthesized. The copolymer is synthesized using aromatic nucleophilic substitution reaction from decafluorobiphenyl and two dihydroxyl-substituted monomers, fluorinated bis-azobenzene-based phenol derivative, and resorcinol. The chemical structure of the copolymer is characterized using <small><sup>1</sup></small>H, <small><sup>19</sup></small>F NMR, FTIR, Raman and UV/vis spectroscopy techniques. The polymer shows remarkable solubility in organic solvents resulting in the formation of robust, self-supporting films. It displays impressive mechanical characteristics as well as remarkable resistance to thermo-oxidative degradation. Under UV light irradiation, photoisomerization occurs both in solution and in the solid copolymer film. The solid polymer films exhibit intense and stable birefringence changes upon the irradiation, enabling the fabrication of diffraction gratings. The study indicates that this synthetic approach is a simple and effective method for designing light-responsive materials.</p>\",\"PeriodicalId\":91,\"journal\":{\"name\":\"Molecular Systems Design & Engineering\",\"volume\":\" 2\",\"pages\":\" 149-157\"},\"PeriodicalIF\":3.2000,\"publicationDate\":\"2023-11-07\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Molecular Systems Design & Engineering\",\"FirstCategoryId\":\"5\",\"ListUrlMain\":\"https://pubs.rsc.org/en/content/articlelanding/2024/me/d3me00150d\",\"RegionNum\":3,\"RegionCategory\":\"工程技术\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, PHYSICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Molecular Systems Design & Engineering","FirstCategoryId":"5","ListUrlMain":"https://pubs.rsc.org/en/content/articlelanding/2024/me/d3me00150d","RegionNum":3,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
Development of a light-responsive fluorinated poly(arylene ether) copolymer containing azobenzene groups in the main polymer chain†
A novel light-responsive poly(arylene ether) copolymer with both azobenzene and perfluorinated biphenylene units as well as meta-linked fragments in the main polymer chain is synthesized. The copolymer is synthesized using aromatic nucleophilic substitution reaction from decafluorobiphenyl and two dihydroxyl-substituted monomers, fluorinated bis-azobenzene-based phenol derivative, and resorcinol. The chemical structure of the copolymer is characterized using 1H, 19F NMR, FTIR, Raman and UV/vis spectroscopy techniques. The polymer shows remarkable solubility in organic solvents resulting in the formation of robust, self-supporting films. It displays impressive mechanical characteristics as well as remarkable resistance to thermo-oxidative degradation. Under UV light irradiation, photoisomerization occurs both in solution and in the solid copolymer film. The solid polymer films exhibit intense and stable birefringence changes upon the irradiation, enabling the fabrication of diffraction gratings. The study indicates that this synthetic approach is a simple and effective method for designing light-responsive materials.
期刊介绍:
Molecular Systems Design & Engineering provides a hub for cutting-edge research into how understanding of molecular properties, behaviour and interactions can be used to design and assemble better materials, systems, and processes to achieve specific functions. These may have applications of technological significance and help address global challenges.