首页> 外文期刊>Designed Monomers and Polymers >Synthesis and homopolymerization kinetics of 7-(methacroyloxy)-2-oxo-heptylphosphonic acid and its copolymerization with methyl methacrylate
【24h】

Synthesis and homopolymerization kinetics of 7-(methacroyloxy)-2-oxo-heptylphosphonic acid and its copolymerization with methyl methacrylate

机译:7-(甲基丙烯酰氧基)-2-氧-庚基膦酸的合成,均聚动力学及其与甲基丙烯酸甲酯的共聚

获取原文
获取外文期刊封面目录资料

摘要

The synthesis of polymerizable 7-(methacroyloxy)-2-oxo-heptylphosphonic acid M1 destined for self-etch adhesives is described. M1 is characterized by ~(1)H, ~(13)C and ~(31)P-NMR spectroscopy. Its homopolymerization and copolymerization reactivity in the solvents methanol and dioxane between 45 and 70°C in the presence of azobisisobutyronitrile (AIBN) are examined. Polymerization proceeds readily through a thermal free radical initiation. The intensity exponents for the monomer and initiator are only slightly over 1 and approximately 0.5, respectively. This is in accordance with the results typically observed for an ideal free radical polymerization with termination mainly by disproportionation, which is typical for methyl methacrylate (MMA) homopolymerization. The kinetics of copolymerization with MMA are monitored by online ~(1)H-NMR spectroscopy. Two copolymerization reactions for each pair of co-monomers are sufficient to evaluate the copolymerization parameters using the Jaacks method, the Fineman–Ross method and the nonlinear least-squares method. All three methods give similar results for particular monomer M1/MMA couple.
机译:描述了用于自蚀刻粘合剂的可聚合7-(甲基丙烯酰氧基)-2-氧-庚基膦酸M1的合成。 M1的特征在于〜(1)H,〜(13)C和〜(31)P-NMR光谱。在偶氮二异丁腈(AIBN)存在下,考察了其在45-70°C的溶剂甲醇和二恶烷中的均聚和共聚反应性。聚合通过热自由基引发而容易进行。单体和引发剂的强度指数分别仅略微超过1和大约0.5。这与理想的自由基聚合反应通常观察到的结果一致,理想的自由基聚合反应主要通过歧化作用终止,这是甲基丙烯酸甲酯(MMA)均聚反应的典型现象。通过在线〜(1)H-NMR光谱监测与MMA共聚的动力学。每对共聚单体的两个共聚反应足以使用Jaacks方法,Fineman-Ross方法和非线性最小二乘法评估共聚参数。对于特定的单体M1 / MMA对,所有这三种方法均给出相似的结果。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号