Short Amy L, Fang Cheng, Nowalk Jamie A, Weiss Ryan M, Liu Peng, Meyer Tara Y
Department of Chemistry, University of Pittsburgh, Pittsburgh, Pennsylvania 15260, United States.
Computational Modeling & Simulation Program, University of Pittsburgh, Pittsburgh, Pennsylvania 15260.
ACS Macro Lett. 2018 Jul 17;7(7):858-862. doi: 10.1021/acsmacrolett.8b00460. Epub 2018 Jun 29.
The hydrolytic behavior and physical properties of a polymer are directly related to its constituent monomer sequence, yet the scalable and controllable synthesis of sequenced copolymers remains scarcely realized. To address this need, an enhanced version of entropy-driven ring-opening metathesis polymerization (ED-ROMP) has been developed. An unprecedented level of control is obtained by exploiting the kinetic and thermodynamic differences in the metathesis activity of - and -olefins embedded in large, unstrained macrocycles. First-order rate kinetics were observed, and polymer molecular weights were found to be proportional to catalyst loading. Computational analysis suggests that incorporation of a olefin into the monomer backbone both introduces a thermodynamic driving force and increases the population of metathesis-active conformers. This approach offers a generally applicable method for enhancing living character in ED-ROMP.
聚合物的水解行为和物理性质与其组成单体序列直接相关,但序列共聚物的可扩展且可控合成仍几乎未实现。为满足这一需求,已开发出一种增强版的熵驱动开环易位聚合(ED-ROMP)。通过利用嵌入大的、无张力大环中的α-和ω-烯烃易位活性的动力学和热力学差异,获得了前所未有的控制水平。观察到一级速率动力学,并且发现聚合物分子量与催化剂负载量成正比。计算分析表明,将α-烯烃引入单体主链既引入了热力学驱动力,又增加了易位活性构象的数量。这种方法提供了一种普遍适用的方法来增强ED-ROMP中的活性特征。