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Synthesis of ethylene oxide methyl methacrylate diblock copolymers by group transfer polymerization of methyl methacrylate with poly(ethylene oxide) macroinitiators

机译:甲基丙烯酸甲酯与聚环氧乙烷大分子引发剂的基团转移聚合反应合成环氧乙烷甲基丙烯酸甲酯二嵌段共聚物

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Ethylene oxide/methyl methacrylate diblock copolymers were prepared by group transfer polymerization (GTP) of methyl methacrylate (MMA) with poly(ethylene oxide) macroinitiators (1). The macroinitiator containing silyl ketene acetal end-groups was synthesized by hydrosilation of poly(ethylene glycol) monomethacrylate which was previously prepared by esterification of poly(ethylene glycol) monomethyl ether (PEO-OH). All synthesized macroinitiators initiated the GTP of MMA in tetrahydrofuran with tetrabutylammonium cyanide or tris(dimethylamino)sulfonium difluoride as catalysts. The polymerization proceeds rapidly at room temperature to quantitative yield. The block copolymers are contaminated with small fractions of PEO homopolymer as a result of uncomplete macroinitiator synthesis. Unreacted PEO-OH, which is present in very small amounts, reduces the concentration of active centers. Therefore, the degree of polymerization is not in good agreement with the theoretical value calculated for a living polymerization taking the monomer to macroinitiator ratio. However, after extraction of the PEO homopolymer, the block copolymers show a narrow molecular weight distribution. Induction periods in time-conversion curves obtained with 1 as initiator vanished nearly, when the reaction was started with the addition product of 1 and MMA. This is an indication, that in the system under investigation a slow initiation step between 1 and the first MMA unit precedes the propagation reaction. Tacticity measurements yield about 56% syndiotactic, 40% heterotactic and 4% isotactic triads for PMMA in the block copolymers. [References: 15]
机译:环氧乙烷/甲基丙烯酸甲酯二嵌段共聚物是通过甲基丙烯酸甲酯(MMA)与聚环氧乙烷大分子引发剂(1)的基团转移聚合(GTP)制备的。含有甲硅烷基乙烯酮缩醛端基的大分子引发剂是由聚乙二醇单甲基丙烯酸酯的硅氢化反应合成的,该聚甲基丙烯酸乙二醇酯是事先通过聚乙二醇单甲醚(PEO-OH)的酯化反应制备的。所有合成的大分子引发剂均以四丁基氰化铵或三(二甲基氨基)二氟化ulf作为催化剂引发了四氢呋喃中MMA的GTP。聚合在室温下快速进行至定量收率。由于不完全的大分子引发剂合成,嵌段共聚物被少量的PEO均聚物污染。少量存在的未反应PEO-OH会降低活性中心的浓度。因此,聚合度与以单体与大分子引发剂的比例进行的活性聚合计算的理论值不一致。然而,在提取PEO均聚物之后,该嵌段共聚物显示出窄的分子量分布。当以1和MMA的加成产物开始反应时,以1作为引发剂获得的时间转换曲线中的诱导期几乎消失。这表明在所研究的系统中,在1和第一个MMA单元之间有一个缓慢的引发步骤,然后才开始传播反应。嵌段共聚物中,PMMA的立构规整度测量得出约56%的间规,40%的杂规和4%的等规三单元组。 [参考:15]

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