| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5201926 | Polymer Degradation and Stability | 2014 | 6 Pages |
Abstract
Enantiomerically pure lactides of l-lactide (LLA) and d-lactide (DLA) were synthesized with high yield (68.5-69.5%) via depolymerization of oligo-poly-l-lactic acid (O-PLLA) and oligo-poly-d-lactic acid (O-PDLA) catalyzed by biogenic creatinine (CR). The structures of synthesized LLA and DLA were characterized with XRD analysis of the prepared single crystals. Gas chromatograph (with a chiral stationary phase capillary column) analysis demonstrated that the synthesized LLA and DLA possessed enantiomeric excess of 100%. The catalytic efficiency of the catalyst creatinine reached to a high level as observed by the turnover frequency in the range of 338.0-347.7Â hâ1. The residues of the depolymerization were utilized for resynthesizing of the enantiomerically pure lactides for 3 circles without the decrease in the yields of enantiomerically pure LLA/DLA. The catalyst we used in this research was biogenic and the process for lactide synthesis featured a closed-cycle without any waste release. A possible mechanism of CR-catalyzed LLA/DLA synthesis was proposed and discussed.
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Wei Huang, Yunbiao Qi, Na Cheng, Xupeng Zong, Tianrong Zhang, Wei Jiang, Hong Li, Quanxing Zhang,
