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End Group Stability of Atom Transfer Radical Polymerization (ATRP)-Synthesized Poly(N-isopropylacrylamide): Perspectives for Diblock Copolymer Synthesis

机译:原子转移自由基聚合(ATRP)合成的聚(N-异丙基丙烯酰胺)的端基稳定性:二嵌段共聚物合成的前景

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摘要

Studies on the end group stability of poly(N-isopropylacrylamide) during the atom transfer radical polymerization (ATRP) process are presented. Polymerization of N-isopropylacrylamide was conducted in different solvents using a copper(I) chloride/Me6Tren catalyst complex. The influence of the ATRP solvent as well as the polymer purification process on the end group stability was investigated. For the first time, mass spectrometry results clearly underline the loss of ω end groups via an intramolecular cyclization reaction. Furthermore, an ATRP system based on a copper(I) bromide/Me6Tren catalyst complex was introduced, that showed not only good control over the polymerization process, but also provided the opportunity of block copolymerization of N-isopropylacrylamide with acrylates and other N-substituted acrylamides. The polymers were characterized using 1H-NMR spectroscopy and size exclusion chromatography. Polymer end groups were determined via ESI-TOF mass spectrometry enhanced by ion mobility separation (IMS).
机译:提出了在原子转移自由基聚合(ATRP)过程中聚(N-异丙基丙烯酰胺)端基稳定性的研究。使用氯化铜(I)/ Me6Tren催化剂配合物在不同溶剂中进行N-异丙基丙烯酰胺的聚合。研究了ATRP溶剂以及聚合物纯化工艺对端基稳定性的影响。质谱分析结果首次明确强调了通过分子内环化反应损失ω端基的现象。此外,引入了基于溴化铜(I)/ Me6Tren催化剂配合物的ATRP系统,该系统不仅显示出对聚合过程的良好控制,而且还提供了N-异丙基丙烯酰胺与丙烯酸酯和其他N-取代嵌段聚合的机会。丙烯酰胺。使用 1 1H-NMR谱和尺寸排阻色谱对聚合物进行表征。聚合物端基通过离子迁移分离(IMS)增强的ESI-TOF质谱测定。

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