School of Chemistry, University of Bristol, Bristol BS8 1TS, UK.
Department of Chemistry, University of Toronto, Toronto, Ontario M5S 3H6, Canada.
Science. 2015 Mar 20;347(6228):1329-32. doi: 10.1126/science.1261816.
Self-assembly of molecular and block copolymer amphiphiles represents a well-established route to micelles with a wide variety of shapes and gel-like phases. We demonstrate an analogous process, but on a longer length scale, in which amphiphilic P-H-P and H-P-H cylindrical triblock comicelles with hydrophobic (H) or polar (P) segments that are monodisperse in length are able to self-assemble side by side or end to end in nonsolvents for the central or terminal segments, respectively. This allows the formation of cylindrical supermicelles and one-dimensional (1D) or 3D superstructures that persist in both solution and the solid state. These assemblies possess multiple levels of structural hierarchy in combination with existence on a multimicrometer-length scale, features that are generally only found in natural materials.
两亲性分子和嵌段共聚物胶束的自组装是一种成熟的方法,可以得到具有各种形状和凝胶相的胶束。我们展示了一种类似的过程,但在更长的长度尺度上,其中疏水性(H)或极性(P)段单分散的两亲性 P-H-P 和 H-P-H 圆柱型三嵌段共聚物胶束能够分别在中心或末端段的非溶剂中并排或端对端自组装。这允许形成圆柱超胶束以及一维(1D)或三维(3D)超结构,这些超结构在溶液和固态中都能稳定存在。这些组装体具有多层次的结构层次,结合存在于多微米长度尺度上,这是通常只在天然材料中才有的特征。