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Low-temperature and purification-free stereocontrolled ring-opening polymerisation of lactide in supercritical carbon dioxide

机译:超临界二氧化碳中的丙交酯的低温和无纯化的立体控制开环聚合

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摘要

A stereoselective, solvent-free ring-opening polymerisation (ROP) of lactide (LA) in supercritical carbon dioxide (scCO(2)) is reported for the first time. The key aim is to exploit scCO(2) to lower the temperature of traditional melt polymerisations, lowering the energy requirement and leading to cleaner polymeric materials. We have utilised a zirconium amine-trisphenolate initiator-stereoselective catalyst [((PrO)-Pr-i)Zr(OPh(Bu-t)(2)-CH2)(3)N] to yield highly heterotactic poly(lactide) (PLA) homopolymer (P-r = 0.74-0.84) from rac-LA, demonstrating control of the PLA microstructure in scCO(2). In addition, high monomer conversion (86-93%) was achieved in short reaction time (1 h), affording poly(lactide) with a very low degree of transesterification and narrow molecular weight distribution. Most importantly, all the reactions were performed at only 80 degrees C, almost 100 degrees C lower than the conventional melt process (typically performed at 130-180 degrees C), representing a very significant potential energy saving.
机译:首次报道了超临界二氧化碳(SCCO(2))中丙交酯(LA)的立体选择性,无溶剂环开环聚合(ROP)。关键目标是利用SCCO(2)来降低传统熔融聚合的温度,降低能量要求并导致清洁剂聚合物材料。我们利用锆胺 - 三苯胺酸盐引发剂 - 立体选择催化剂[((Pro)-PR-I)Zr(OPH(BU-T)(2)-CH2)(3)N],得到高度异象性聚(丙交酯)( PLA)来自RAC-LA的均聚物(PR = 0.74-0.84),证明了SCCO(2)中PLA微观结构的控制。此外,在短反应时间(1小时)中实现高单体转化(86-93%),得到聚(丙交酯),具有非常低的酯交换和窄分子量分布。最重要的是,所有反应仅在80℃下进行,几乎100摄氏度低于传统熔体工艺(通常在130-180℃),表示非常显着的潜在节能。

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