Department of Polymer Chemistry, Graduate School of Engineering, Kyoto University, Katsura, Nishikyo-ku, Kyoto 615-8510, Japan.
Nat Commun. 2013;4:2321. doi: 10.1038/ncomms3321.
Cyclopolymerization is a chain polymerization of bifunctional monomers via alternating processes of intramolecular cyclization and intermolecular addition, to give soluble linear polymers consisting of in-chain cyclic structures. Though cyclopolymers comprising in-chain multiple large rings potentially show unique functionality, they generally require the elaborate design of bifunctional monomers. Here we report cation template-assisted cyclopolymerization of poly(ethylene glycol) dimethacrylates as an efficient strategy directly yielding polymeric pseudo-crown ethers with large in-chain cavities (up to 30-membered rings) for selective molecular recognition. The key is to select a size-fit metal cation for the spacer unit of the divinyl monomers to form a pseudo-cyclic conformation, where the two vinyl groups are suitably positioned for intramolecular cyclization. The marriage of supramolecular chemistry and polymer chemistry affords efficient, one-pot chemical transformation from common chemical reagents with simple templates to functional cyclopolymers.
环化聚合是通过分子内环化和分子间加成的交替过程对双官能单体进行的链式聚合,得到由链内环状结构组成的可溶性线性聚合物。尽管包含链内多个大环的环聚合物可能具有独特的功能,但它们通常需要精心设计双官能单体。在这里,我们报告了阳离子模板辅助的聚乙二醇二甲基丙烯酸酯的环化聚合,这是一种直接生成具有大链内空腔(高达 30 元环)的聚合型拟冠醚的有效策略,用于选择性分子识别。关键是选择合适尺寸的金属阳离子作为二乙烯基单体的间隔基,以形成拟环构象,其中两个乙烯基基团适当地定位进行分子内环化。超分子化学和聚合物化学的结合提供了一种有效的一锅化学转化方法,可从简单模板的常见化学试剂中获得功能化的环聚合物。