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Advances in the (co)polymerization of alkyl 2-trifluoromethacrylates and 2-(trifluoromethyl)acrylic acid

机译:2-三氟甲基丙烯酸烷基酯与2-(三氟甲基)丙烯酸的(共)聚合研究进展

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This review reports an overview on the synthesis, polymerizability, uses, and applications of alkyl 2-trifluoromethacrylate (or α-trifluoromethacrylate) monomers. Alkyl 2-trifluoromethacrylate (where the alkyl group stands for methyl, ethyl, or t-butyl) and 2-(trifluoromethyl)acrylic acid are very important comonomers and their copolymers or terpolymers have drawn a lot of interest in High-Tech applications as well as their low toxicity, easy availability and easy handling which make them versatile comonomers and materials. First, several strategies on the preparation of such monomers mainly from 3,3,3-trifluoropropene are summarized. These monomers can further lead to various original monomers bearing functional groups such as epoxide, cyclic ethers, oligo(ethylene oxide), or perfluorinated group, and others. As highly electron-withdrawing monomers, alkyl 2-trifluoromethacrylate and 2-(trifluoromethyl)acrylic acid can easily be homopolymer-ized under anionic conditions but several studies reported that the homopolymerization failed from radical initiators. However, homopolymerization of 2-(trifluoromethyl)acrylic acid has recently been achieved under specific radical and pH conditions successfully. Moreover, the radical copolymerizations of alkyl 2-trifluoromethacrylate and 2-(trifluoromethyl)acrylic acid with electron-donating hydrogenated monomers such as a-olefins, vinyl ethers, styrene, and norbornenes led to a wide range of alternating copolymers. More recently, the conventional radical (co)polymerization or (ter)polymerization of these monomers with fluorinated monomers (such as 2,2,2-trifluoroethyl methacrylate, 2,2,2-trifluoroethyl α-fluoroacrylate, hexafluoropropylene, fluorinated vinyl ethers or vinylidene fluoride, VDF) has enabled to obtain original fluoropolymers. In addition, the controlled radical copolymerizations of these α-trifluoromethyl containing monomers with VDF were successfully achieved by different techniques and could promote original syntheses of block copolymers. Materials resulting from these monomers are useful in the field of lithography, molecularly imprinted polymers, optics, adsorbants, polymer electrolyte membranes for fuel cell, lithium ion batteries, protective stone coatings, multicompartmental micelles, and nanocomposites.
机译:这篇评论报告了2-三氟甲基丙烯酸烷基酯(或α-三氟甲基丙烯酸酯)单体的合成,可聚合性,用途和应用的概述。 2-三氟甲基丙烯酸烷基酯(烷基代表甲基,乙基或叔丁基)和2-(三氟甲基)丙烯酸是非常重要的共聚单体,它们的共聚物或三元共聚物也引起了高科技领域的关注由于它们的低毒性,易得性和易处理性,使其成为通用的共聚单体和材料。首先,总结了主要由3,3,3-三氟丙烯制备此类单体的几种策略。这些单体可以进一步导致带有官能团例如环氧化物,环醚,低聚(环氧乙烷)或全氟基团等的各种原始单体。作为高吸电子单体,2-三氟甲基丙烯酸烷基酯和2-(三氟甲基)丙烯酸可以很容易地在阴离子条件下均聚,但是有几项研究报告称,自由基引发剂导致均聚失败。然而,最近在特定的自由基和pH条件下成功地实现了2-(三氟甲基)丙烯酸的均聚。此外,烷基2-三氟甲基丙烯酸酯和2-(三氟甲基)丙烯酸与给电子氢化单体如α-烯烃,乙烯基醚,苯乙烯和降冰片烯的自由基共聚导致了广泛的交替共聚物。最近,这些单体与氟化单体(例如2,2,2-三氟乙基甲基丙烯酸酯,2,2,2-三氟乙基α-氟丙烯酸酯,六氟丙烯,氟化乙烯基醚或氟代乙烯基酯)的常规自由基(共)聚合或(三)聚合。偏二氟乙烯(VDF)已能够获得原始的含氟聚合物。另外,这些含α-三氟甲基的单体与VDF的受控自由基共聚通过不同的技术成功实现,并且可以促进嵌段共聚物的原始合成。由这些单体得到的材料可用于光刻,分子印迹聚合物,光学器件,吸附剂,用于燃料电池的聚合物电解质膜,锂离子电池,保护性石材涂层,多隔室胶束和纳米复合材料领域。

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