RIKEN Center for Emergent Matter Science, 2-1 Hirosawa, Wako, Saitama 351-0198, Japan. Department of Chemistry and Biotechnology, School of Engineering, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo 113-8656, Japan.
RIKEN Center for Emergent Matter Science, 2-1 Hirosawa, Wako, Saitama 351-0198, Japan.
Science. 2015 Feb 6;347(6222):646-51. doi: 10.1126/science.aaa4249.
Over the past decade, major progress in supramolecular polymerization has had a substantial effect on the design of functional soft materials. However, despite recent advances, most studies are still based on a preconceived notion that supramolecular polymerization follows a step-growth mechanism, which precludes control over chain length, sequence, and stereochemical structure. Here we report the realization of chain-growth polymerization by designing metastable monomers with a shape-promoted intramolecular hydrogen-bonding network. The monomers are conformationally restricted from spontaneous polymerization at ambient temperatures but begin to polymerize with characteristics typical of a living mechanism upon mixing with tailored initiators. The chain growth occurs stereoselectively and therefore enables optical resolution of a racemic monomer.
在过去的十年中,超分子聚合的重大进展对功能软物质的设计产生了重大影响。然而,尽管最近取得了进展,但大多数研究仍然基于这样一种先入为主的观念,即超分子聚合遵循逐步增长的机制,这使得无法控制链长、序列和立体化学结构。在这里,我们通过设计具有形状促进的分子内氢键网络的亚稳态单体来实现链式聚合。在环境温度下,这些单体受到构象限制而无法自发聚合,但在与定制引发剂混合后,它们开始聚合,表现出典型的活性聚合机制的特征。链增长具有立体选择性,因此能够对消旋单体进行光学拆分。