Optimizing Activators Regenerated by Electron Transfer for Atom Transfer Radical Polymerization of Methyl Methacrylate Initiated by Ethyl 2-bromopropionate

Mingsen Chen, H. Zhou, Xiaofang Li, Li Zhou, Faai Zhang
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Abstract

In this study, we used ethyl 2-bromopropionate (EBrP) as an initiator of activators regenerated by electron transfer for atom transfer radical polymerization (ARGET ATRP) of methyl methacrylate (MMA). We investigated in detail the effect on polymerization of different kinds of reducing agents and ligands, the amounts of the reducing agent and catalyst, and reaction temperature. We determined the molecular weight and dispersity of the polymers by gel permeation chromatography (GPC). The results reveal glucose to be the best reducing agent for this system. The monomer conversion increased with increases in the reaction temperature and in the feeding amounts of the reducing agent and catalyst. The optimum amount of the reducing agent and minimal amount of catalyst required depend on the particular system. For example, we polymerized MMA with 200 ppm of catalyst and 15-fold of glucose/CuCl 2 resulting in a PMMA with high M n ( M n,GPC = 48 700, M n,theo = 48 500) and low dispersity (1.27). The first-order kinetics show that the molecular weights increased linearly with the monomer conversion and are consistent with the theoretical values, the chain extension reaction and end group analysis results also demonstrate that the characteristics of polymerization process belong to a typical “living”/controlled radical polymerization. Moreover, 1 H-NMR analysis results indicate the stereoregularity of the polymer is given priority over syndiotactic architecture and the effect of the type of ligand on the stereoregularity is very slight.
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2-溴丙酸乙酯引发甲基丙烯酸甲酯原子转移自由基聚合电子转移再生活化剂的优化
本研究以2-溴丙酸乙酯(EBrP)作为甲基丙烯酸甲酯(MMA)原子转移自由基聚合(ARGET ATRP)电子转移再生活化剂的引发剂。考察了不同还原剂和配体的用量、还原剂和催化剂的用量以及反应温度对聚合反应的影响。用凝胶渗透色谱法测定了聚合物的分子量和分散性。结果表明,葡萄糖是该体系的最佳还原剂。单体转化率随反应温度、还原剂和催化剂投加量的增加而增加。还原剂的最佳用量和催化剂的最小用量取决于具体的体系。例如,我们用200 ppm的催化剂和15倍的葡萄糖/CuCl 2聚合MMA,得到高mn (mn,GPC = 48 700, mn,theo = 48 500)和低分散性(1.27)的PMMA。一级动力学结果表明,分子量随单体转化率的增加而线性增加,与理论值一致;延伸链反应和端基分析结果也表明聚合过程属于典型的 - œlivingâ - > /可控自由基聚合。1h - nmr分析结果表明,聚合物的立体规整性比共规性更重要,配体类型对聚合物的立体规整性影响很小。
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