Department of Chemistry, Imperial College London , London SW7 2AZ, U.K.
Department of Chemistry, University of Bath , Bath BA2 7AY, U.K.
J Am Chem Soc. 2016 Mar 30;138(12):4120-31. doi: 10.1021/jacs.5b13070. Epub 2016 Mar 22.
Controlling polymer composition starting from mixtures of monomers is an important, but rarely achieved, target. Here a single switchable catalyst for both ring-opening polymerization (ROP) of lactones and ring-opening copolymerization (ROCOP) of epoxides, anhydrides, and CO2 is investigated, using both experimental and theoretical methods. Different combinations of four model monomers-ε-caprolactone, cyclohexene oxide, phthalic anhydride, and carbon dioxide-are investigated using a single dizinc catalyst. The catalyst switches between the distinct polymerization cycles and shows high monomer selectivity, resulting in block sequence control and predictable compositions (esters and carbonates) in the polymer chain. The understanding gained of the orthogonal reactivity of monomers, specifically controlled by the nature of the metal-chain end group, opens the way to engineer polymer block sequences.
从单体混合物出发控制聚合物组成是一个重要但很少实现的目标。在这里,我们通过实验和理论方法研究了一种可同时用于开环聚合(ROP)内酯和开环共聚(ROCOP)环氧化物、酸酐和 CO2 的单种可切换催化剂。使用单一的二锌催化剂研究了四种模型单体(ε-己内酯、环己烯氧化物、邻苯二甲酸酐和二氧化碳)的不同组合。催化剂在不同聚合循环之间切换,并表现出高单体选择性,从而实现嵌段序列控制和聚合物链中可预测的组成(酯和碳酸酯)。对单体正交反应性的理解,特别是受金属链端基性质控制,为设计聚合物嵌段序列开辟了道路。