Graduate School of Chemical Sciences and Engineering, and Faculty of Engineering, Hokkaido University, Sapporo, 060-8628, Japan.
Chem Commun (Camb). 2014 Mar 18;50(22):2883-5. doi: 10.1039/c4cc00215f. Epub 2014 Feb 3.
A high enantiomer-selectivity for the polymerization of rac-lactide was achieved using chiral binaphthol-derived monophosphoric acids as organocatalysts. During the polymerization, d-lactide (DLA) preferentially polymerized via kinetic resolution with the maximum selectivity factor (kD/kL) of 28.3. The selective polymerization of DLA was derived from a dual activation, i.e., monomer activation and chain-end activation.
手性联萘酚衍生的单磷酸作为有机催化剂实现了 rac-丙交酯聚合的高对映选择性。在聚合过程中,d-丙交酯(DLA)通过动力学拆分优先聚合,最大选择性因子(kD/kL)为 28.3。DLA 的选择性聚合源自双重活化,即单体活化和链端活化。