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Atom transfer radical polymerization of methylmethacrylate and styrene initiated by 3,5-bis(perfluorobenzyloxy)benzyl 2-bromopropanoate

机译:甲基丙烯酸甲酯和苯乙烯的原子转移自由基聚合反应由3,5-双(全氟苄氧基)苄基2-溴丙酸酯引发

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摘要

The synthesis of polymethylmethacrylate (pMMA) and polystyrene (pSt) were realized with newly synthesized initiator, 3,5-bis(perfluorobenzyloxy)benzyl 2-bromopropanoate (FBr) in the presence of copper bromide (CuBr) and N,N,N',N'', N''-pentamethyl-diethylenetriamine (PMDETA) by using atom transfer radical polymerization (ATRP). The perfluorinated aromatic group containing initiator was prepared by esterification of the (3,5-bis(perfluorobenzyl)oxy-phenyl alcohol. Both initiator and polymers were characterized by ~1H-NMR spectroscopy, gel permeation chromatography, differential scanning calorimetry, and thermogravimetric analysis. The ATRP was supported by an increase in the molecular weight of the forming polymers and also by their monomodal molecular weight distribution. Contact angle measurements of water and ethylene glycol on films of synthesized polymers indicated higher degree of hydrophobicity than that of pure pMMA and pure pSt.
机译:采用原子转移自由基聚合(ATRP)技术,以新合成的引发剂3,5-双(全氟苄氧基)苄基2-溴丙酸酯(FBr)和N,N,N',N'',N''-五甲基二乙烯三胺(PMDETA)为原料,合成了聚甲基丙烯酸甲酯(pMMA)和聚苯乙烯(pSt)。由(3,5-双[(全氟苄基)氧基]-苯醇酯化制备了含全氟芳香族引发剂。采用~1H-NMR波谱、凝胶渗透色谱、差示扫描量热和热重分析等手段对引发剂和聚合物进行了表征。ATRP得到了形成聚合物分子量的增加以及它们的单峰分子量分布的支持。水和乙二醇在合成聚合物薄膜上的接触角测量表明,其疏水性高于纯pMMA和纯pSt。

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