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Synthesis of poly(methylmethacrylate) macromonomers prepared by radical chain transfer reaction H NMR study of macromonomer end-groups

机译:自由基链转移反应制备的聚甲基丙烯酸甲酯大分子单体的合成1 H NMR研究大单体端基

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摘要

The end-group analysis for both PMMA telomers having a carboxyl end-group and macromonomers derived from these telomers was carried out using ~1H NMR. Telomers were prepared by telomerization of methyl methacryalte (MMA) with thioglycolic acid (TGA) initated with 2,2' azobis(isobutyronitrile) (AIBN) in acetontrile at 70 deg C. Then, macromonomers were obtained by reaction of the telomer carboxylic acid end-group with glycidyl methacrylate (GMA) using a chromium salt as catalyst. From the ~1H NMR study, it was found that the telomer/macromonomer conversion results from two ways of epoxy addition (#alpha# and #beta#), as observed in a model reaction between GMA and octanoic acid (OA).
机译:使用〜1H NMR对具有羧基端基的PMMA端粒和衍生自这些端粒的大分子单体进行端基分析。甲基丙烯酸甲酯(MMA)与巯基乙酸(TGA)的端粒聚合反应在70℃下于乙腈中用2,2'偶氮二(异丁腈)(AIBN)引发。然后,通过端粒羧酸末端的反应获得大分子单体-使用铬盐作为催化剂的甲基丙烯酸缩水甘油酯(GMA)基团。从〜1H NMR研究中,发现端粒/大分子单体转化是由两种环氧加成方式(#alpha#和#beta#)导致的,这是在GMA和辛酸(OA)之间的模型反应中观察到的。

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