2009/01/26 by Noureddine Ajellal, M. Bouyahyi, Miloud Bouyahyi +9 · 3 citations
Materials Science · Chemical Engineering · #biodegradable polymer synthesis and properties #Carbon dioxide utilization in catalysis #Polymer crystallization and properties
paper · doi:10.1021/ma8022734
The mechanism of the ring-opening polymerization of rac -β-butyrolactone using yttrium complexes supported by dianionic aminoalkoxybis(phenolate) ligands as initiators has been investigated by NMR and shown to occur via a coordination-insertion pathway. The microstructure of the resulting syndiotactic-enriched poly(3-hydroxybutyrate)s (PHBs, P r up to 0.94) has been studied by 13 C NMR spectroscopy, enabling a detailed assignment of resonances at the diad and triad levels. On this basis, a statistical Bernoullian analysis has been performed which evidenced that syndioselectivity originates from a chain-end control. Some thermal properties of these PHBs have been studied by WAXD and thermoanalytical techniques and shown to be markedly affected by the syndiotacticity degree. This is especially the case for the melting temperature which raises up to 183 °C for P r = 0.94, a temperature higher than that of pure isotactic PHB (ca. 180 °C).