首页> 外文期刊>Polymer bulletin >Synthesis of poly(#epsilon#-carprolactone-b-isobutylene)diblock copolymer and poly(#epsilon#-caprolactone-b-isobutylene-b-#epsilon#-caprolctone)triblock copolymer
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Synthesis of poly(#epsilon#-carprolactone-b-isobutylene)diblock copolymer and poly(#epsilon#-caprolactone-b-isobutylene-b-#epsilon#-caprolctone)triblock copolymer

机译:聚(εε-己内酯-b-异丁烯)二嵌段共聚物和聚(εε-己内酯-b-异丁烯-b-εε-己内酯)三嵌段共聚物的合成

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摘要

Poly(isobutylene-b-#epsilon#-caprolactone)diblock and poly(#epsilon#-caprolactone-b-isobutylene-b-#epsilon#-caprolctone)triblock copolymers have been prepared and characterized.The synthesis involved the living cationic polymerizationh of IB,followed by capping with 1,1-diphenylethylene or 1,1-p-ditolylethylene and end-quenchign with 1-methoxy-1-trimethylsiloxy-2-methyl-propene to yield methoxycarbonyl functional PIB.Hydroxyl end-functional PIB polymers were quantittively obtained by the subsequent reduction of methoxycarbonyl end-functional PIB with LiAlH_4.The structure of hydroxyl end-functional PIBs was confirmed by ~1H NMR and IR spectroscopy.Poly(#epsilon#-caprolactone-b-isobutylene)diblock copolymers and poly(#epsilon#-caprolactone-b-isobutylene-b-#epsilon#-caprolactone)triblock copolymers were synthesized by the living cationic ring-opening polymerization of #epsilon#-carpolactone with hydroxyl end-fucntional PIB as macroinitiator in the presence of HCl·Et_2O via the "activated monomer mechanism".The block copolymers exhibited close to theoretical M_ns and narrow molecular weight distributions.
机译:制备并表征了聚(异丁烯-b-ε-己内酯)二嵌段共聚物和聚(ε-己内酯-b-异丁烯-b-ε-己内酯)三嵌段共聚物。 IB,接着用1,1-二苯基乙烯或1,1-对二甲苯基乙烯封端,并用1-甲氧基-1-三甲基甲硅烷氧基-2-甲基丙烯进行淬灭,得到甲氧基羰基官能的PIB。通过随后用LiAlH_4还原甲氧基羰基端基PIB定量获得。羟基端基PIBs的结构通过〜1H NMR和IR光谱证实。以盐酸端基PIB为大分子引发剂,通过#ε-己内酯的阳离子阳离子开环聚合反应,合成了ε-己内酯-异丁烯-β-ε-己内酯三嵌段共聚物。 Et_2O通过“已激活嵌段共聚物表现出接近理论的M_ns和窄的分子量分布。

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