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

Gokhan Sagdic, U. Gunay
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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
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
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