Institut des Biomolécules Max Mousseron, UMR5247 CNRS, Université Montpellier 1 et 2, 15 Avenue Charles Flahault, 34000 Montpellier, France.
Macromol Rapid Commun. 2011 Jun 16;32(12):876-80. doi: 10.1002/marc.201100235. Epub 2011 May 20.
A new strategy for the synthesis of polyamides from polyesters of hydroxyl-containing amino acids using a multi O-N acyl transfer reaction was developed. This original approach allowed the synthesis of three generations of polymers from the same starting monomer. The polymerization of N-benzyloxycarbonyl-serine and its γ-homologated derivative provided the Z-protected polyesters; then the water-soluble polycationic polyesters were obtained by removal of the Z-protecting group; and finally the polyamides were obtained by a base-induced multi O-N acyl transfer, both in aqueous or organic medium. The key step transfer reaction was monitored by the disappearance and appearance of characteristic NMR proton signals and IR bands of polyesters and polyamides.
开发了一种使用多 O-N 酰基转移反应从含羟基氨基酸的聚酯合成聚酰胺的新策略。这种新颖的方法允许从相同的起始单体合成三代聚合物。N-苄氧羰基-丝氨酸及其 γ-同系物的聚合提供了 Z-保护聚酯;然后通过去除 Z-保护基得到水溶性聚阳离子聚酯;最后通过碱诱导的多 O-N 酰基转移得到聚酰胺,既可以在水相也可以在有机相中进行。关键的转移反应步骤通过特征性 NMR 质子信号和聚酯和聚酰胺的 IR 带的消失和出现来监测。