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Synthesis of cross-linkable telechelic poly(butenylene)s derived from ring-opening metathesis polymerization

机译:开环复分解聚合衍生的可交联遥爪聚丁烯的合成

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The synthesis of ring-opening metathesis polymerization (ROMP) chain transfer agents (CTA)s bearing methacrylate or epoxide end functionality was accomplished. In the presence of these CTAs, the ROMP of cyclooctadiene (COD) initiated with (PCy3)(2)Cl2Ru=CHPh afforded the respective telechelic poly(butenylene)s with either methacrylate or epoxide end groups. Control over the polymer molecular weight was demonstrated by varying the COD/CTA ratio; Successful cross-linking by thermal or photochemical initiation of the bis(methacrylate)-functionalized telechelic poly(butenylene)s or through acid catalysis of the bis(epoxide)-functionalized telechelic poly(butenylene)s was accomplished. While crosslinking was found to reduce solubility of the polymers, it greatly enhanced their thermal stability. [References: 35]
机译:完成了带有甲基丙烯酸酯或环氧化物末端官能团的开环复分解聚合(ROMP)链转移剂(CTA)的合成。在这些CTA的存在下,以(PCy3)(2)Cl2Ru = CHPh引发的环辛二烯(COD)的ROMP分别提供了带有甲基丙烯酸酯或环氧端基的远螯聚(丁烯)。通过改变COD / CTA比证明了对聚合物分子量的控制。通过热或光化学引发双(甲基丙烯酸酯)官能化的远螯聚(丁烯)或通过酸催化双(环氧)官能化的远螯聚(丁烯),成功实现了交联。虽然发现交联降低了聚合物的溶解度,但它大大提高了它们的热稳定性。 [参考:35]

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