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端基为巯基的聚己内酯的合成
  • 期刊名称:高等学校化学学报, 2007, V28, 1791~1795
  • 时间:0
  • 分类:O631[理学—高分子化学;理学—化学]
  • 作者机构:[1]北京大学化学与分子工程学院高分子科学与工程系,高分子化学与物理教育部重点实验室,北京100871
  • 相关基金:国家自然科学基金(批准号:50573002)和教育部“新世纪优秀人才支持计划”资助
  • 相关项目:端基为糖基的聚氨基酸的合成及新型药物载体构筑
中文摘要:

以三氟甲烷磺酸亚锡为催化剂,2-巯基乙醇为引发剂,在温和条件下引发ε-己内酯的开环聚合,得到端基为巯基的聚己内酯,其分子量可控且分布较窄.在此过程中,巯基不需要保护而不会影响聚酯的结构,当聚合温度升高时,聚合物端基结构不发生改变,但分子量分布变宽.端基为巯基的聚己内酯能够通过偶合反应生成中间含二硫键的聚己内酯;同时,以2-羟乙基二硫化合物为引发剂合成得到分子中间含二硫键的窄分布聚己内酯,经还原后也可得到端基为巯基的聚己内酯.这两种方法条件温和,效率较高,具有良好的可控性.

英文摘要:

Thiol-terminated poly (ε-caprolactone) (PCL) was synthesized with 2-mercapto ethanol and through two mild, simple and efficient methods : one is the ring-opening polymerization of ε-caprolactone with 2-mercaptoethanol as initiator and stannous ( Ⅱ ) trifluoromethane sulfonate as catalyst; the other is the ring-o- pening polymerization of ε-caprolactone with 2-hydroxyethyl disulfide as initiator, followed by reduction reaction. In the first method, when the polymerization temperature was increased, the molecular weight distribution of the final product was broad, while the structure remained unchanged ; this thio-end capped PCL can be coupled to form a new polymer with a disulfide group in the center. The structures of these polyesters were confirmed by ^1H NMR spectra and gel permeation chromatography. The polymers show controlled molecular weights and narrow molecular weight distributions. These methods may also be used to prepare other polyesters with thiol-end groups.

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