Chen Jianzhuang, Li Nan, Gao Yongping, Sun Fugen, He Jianping, Li Yongsheng
Laboratory of Low-Dimensional Materials Chemistry, School of Materials Science and Engineering, East China University of Science and Technology, Shanghai 200237, P. R. China.
Soft Matter. 2015 Oct 21;11(39):7835-40. doi: 10.1039/c5sm01641j. Epub 2015 Sep 1.
Based on the selective recognition of the polyethylene (PE) block of polyethylene-block-poly(ethylene glycol) (PE-b-PEG) by 1,4-diethoxypillar[5]arene (DEP5A), two novel thermo and competitive guest (1,4-dibromobutane or hexanedinitrile) responsive polypseudorotaxanes (PPRs) have been successfully constructed. The formation of PPRs both in solution and in the solid state was demonstrated by (1)H NMR, 2D NOESY, and WAXD analyses. TGA data illustrate that PPRs exhibit higher thermal stability than their precursor diblock copolymers. Moreover, intriguing porous disk-like aggregates are produced by electrospraying of PPRs in CHCl3 and the self-assembled structures of PPRs are totally changed by the addition of 1,4-dibromobutane or hexanedinitrile, demonstrating their competitive guest stimuli-responsiveness.
基于1,4-二乙氧基柱[5]芳烃(DEP5A)对聚乙二醇-聚(乙二醇)(PE-b-PEG)中聚乙烯(PE)嵌段的选择性识别,成功构建了两种新型的热响应和竞争性客体(1,4-二溴丁烷或己二腈)响应性聚准轮烷(PPR)。通过¹H NMR、二维NOESY和WAXD分析证明了溶液和固态中PPR的形成。热重分析(TGA)数据表明,PPR比其前体二嵌段共聚物具有更高的热稳定性。此外,通过在CHCl₃中电喷雾PPR产生了有趣的多孔盘状聚集体,并且通过添加1,4-二溴丁烷或己二腈,PPR的自组装结构完全改变,证明了它们的竞争性客体刺激响应性。