Schömer Martina, Seiwert Jan, Frey Holger
Institute of Organic Chemistry, Johannes Gutenberg-University, Duesbergweg 10-14, D-55099 Mainz, Germany.
ACS Macro Lett. 2012 Jul 17;1(7):888-891. doi: 10.1021/mz300256y. Epub 2012 Jun 29.
Backbone-thermoresponsive hyperbranched poly(propylene oxide)-based polyether polyols have been synthesized by anionic ring-opening copolymerization of glycidol and propylene oxide. The number of functional hydroxyl end groups and the lower critical solution temperature (LCST) can be readily adjusted by varying the comonomer ratio. Molecular weights in the range of 1200-2000 g/mol were achieved. Hyperbranched polyether polyols with LCST values between 24 and 83 °C can be obtained in a convenient one-step reaction.
通过缩水甘油与环氧丙烷的阴离子开环共聚反应合成了具有主链热响应性的超支化聚环氧丙烷基聚醚多元醇。通过改变共聚单体比例,可以很容易地调节功能性羟基端基的数量和低临界溶液温度(LCST)。实现了1200-2000 g/mol范围内的分子量。通过便捷的一步反应可获得LCST值在24至83℃之间的超支化聚醚多元醇。