Gazzotti Stefano, Ortenzi Marco Aldo, Farina Hermes, Silvani Alessandra
Department of Chemistry, University of Milan, Via Golgi 19, 20133 Milan, Italy.
CRC Materiali Polimerici (LaMPo), Department of Chemistry, University of Milan, Via Golgi 19, 20133 Milan, Italy.
Polymers (Basel). 2020 Oct 18;12(10):2396. doi: 10.3390/polym12102396.
The first example of solvent-free, organocatalyzed, polymerization of 1,3-dioxolan-4-ones, used as easily accessible monomers for the synthesis of polylactic acid (PLA), is described here. An optimization of reaction conditions was carried out, with -toluensulfonic acid emerging as the most efficient Brønsted acid catalyst. The reactivity of the monomers in the tested conditions was studied following the monomer conversion by H NMR and the molecular weight growth by SEC analysis. A double activation polymerization mechanism was proposed, pointing out the key role of the acid catalyst. The formation of acetal bridges was demonstrated, to different extents depending on the nature of the aldehyde or ketone employed for lactic acid protection. The polymer shows complete retention of stereochemistry, as well as good thermal properties and good polydispersity, albeit modest molecular weight.
本文描述了无溶剂、有机催化的1,3 - 二氧戊环 - 4 - 酮聚合反应的首个实例,该反应中1,3 - 二氧戊环 - 4 - 酮用作合成聚乳酸(PLA)的易于获取的单体。进行了反应条件的优化,对甲苯磺酸成为最有效的布朗斯特酸催化剂。通过核磁共振氢谱(¹H NMR)跟踪单体转化率以及通过尺寸排阻色谱(SEC)分析分子量增长情况,研究了测试条件下单体的反应活性。提出了一种双活化聚合机理,指出了酸催化剂的关键作用。证实了缩醛桥的形成,其形成程度取决于用于乳酸保护的醛或酮的性质。该聚合物显示出立体化学的完全保留,以及良好的热性能和良好的多分散性,尽管分子量适中。