Post-polymerization modification of pentafluorophenyl-functionalized polythioether via thiol-para-fluoro click reaction

Gokhan Sagdic, U. Gunay
{"title":"Post-polymerization modification of pentafluorophenyl-functionalized polythioether via thiol-para-fluoro click reaction","authors":"Gokhan Sagdic, U. Gunay","doi":"10.1080/10601325.2023.2227651","DOIUrl":null,"url":null,"abstract":"Abstract In this work, a rapid polymerization method was combined with thiol-para-fluoro (TPF) “click” post-polymerization modification (PPM) strategy. To this end, a reactive monomer, namely bis((perfluorophenyl)methyl) but-2-ynedioate, was specifically designed and used in the synthesis of polythioether via thiol-Michael addition reaction by using 1,6-hexanedithiol (HDT) and 1,5,7-triazabicyclo[4.4.0]dec-5-ene (TBD) as a catalyst, and the reaction proceeded at room temperature for 5 min to give the pristine polythioether P0. This polymer was then used as a platform to perform PPM with various thiol compounds. The PPM reactions showed quantitative efficiency in 4 h with moderate to high yields. All modified polymers were analyzed with 1H, 13C, and 19F NMR analyses, and molecular weights were calculated by using GPC. It is believed that combining such polymerization and PPM reactions can be a very useful tool to obtain polymers having different structures for different purposes. Hence, this work introduces a new type of polymer backbone that can be rapidly prepared and undergo a relatively fast PPM. Graphical Abstract","PeriodicalId":16228,"journal":{"name":"Journal of Macromolecular Science, Part A","volume":"220 1","pages":"548 - 556"},"PeriodicalIF":0.0000,"publicationDate":"2023-06-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Macromolecular Science, Part A","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1080/10601325.2023.2227651","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 1

Abstract

Abstract In this work, a rapid polymerization method was combined with thiol-para-fluoro (TPF) “click” post-polymerization modification (PPM) strategy. To this end, a reactive monomer, namely bis((perfluorophenyl)methyl) but-2-ynedioate, was specifically designed and used in the synthesis of polythioether via thiol-Michael addition reaction by using 1,6-hexanedithiol (HDT) and 1,5,7-triazabicyclo[4.4.0]dec-5-ene (TBD) as a catalyst, and the reaction proceeded at room temperature for 5 min to give the pristine polythioether P0. This polymer was then used as a platform to perform PPM with various thiol compounds. The PPM reactions showed quantitative efficiency in 4 h with moderate to high yields. All modified polymers were analyzed with 1H, 13C, and 19F NMR analyses, and molecular weights were calculated by using GPC. It is believed that combining such polymerization and PPM reactions can be a very useful tool to obtain polymers having different structures for different purposes. Hence, this work introduces a new type of polymer backbone that can be rapidly prepared and undergo a relatively fast PPM. Graphical Abstract
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
巯基-对氟键合反应对五氟苯基功能化聚硫醚的聚合后改性
摘要本研究将一种快速聚合方法与巯基对氟(TPF)“点击”聚合后改性(PPM)策略相结合。为此,专门设计了一种反应单体,即双(全氟苯基)甲基-2-炔酸酯,以1,6-己二硫醇(HDT)和1,5,7-三氮杂环[4.4.0]十二-5-烯(TBD)为催化剂,通过巯基-迈克尔加成反应合成聚硫醚,并在室温下反应5min,得到原始聚硫醚P0。然后将该聚合物用作与各种硫醇化合物进行PPM的平台。PPM反应在4 h内表现出定量效率,产率中高。通过1H、13C和19F NMR分析所有改性聚合物,并通过GPC计算分子量。人们相信,将这种聚合和PPM反应结合起来可以成为一种非常有用的工具,以获得用于不同用途的具有不同结构的聚合物。因此,这项工作介绍了一种新型的聚合物骨架,可以快速制备并进行相对快速的PPM。图形抽象
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Synthesis and characterization of completely amorphous thermal resistant copolyesters based on biomass isosorbide Aromatic (co)polycarbonates bearing pendant 2,3-dimethylmaleimido group based upon a new phthalimidine-containing “cardo” bisphenol Characterization and comparability study of a series of novel fluorinated polyacrylates with a rigid cyclohexane mesogenic core Synthesis and characterization of UV curable polyurethane-acrylate nanocomposite-based coatings enhanced with magnesium fluoride nanoparticles Furan-containing polymer-coated magnetic nanoparticles using the ‘graft-to’ approach
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1