Cui Honggang, Chen Zhiyun, Zhong Sheng, Wooley Karen L, Pochan Darrin J
Department of Materials Science and Engineering and Delaware Biotechnology Institute, University of Delaware, Newark, Delaware 19716, USA.
Science. 2007 Aug 3;317(5838):647-50. doi: 10.1126/science.1141768.
Block copolymers consist of two or more chemically different polymer segments, or blocks, connected by a covalent linkage. In solution, amphiphilic blocks can self-assemble as a result of energetic repulsion effects between blocks. The degree of repulsion, the lengths of the block segments, and the selectivity of the solvent primarily control the resultant assembled morphology. In an ideal situation, one would like to be able to alter the morphology that forms without having to change the chemistry of the block copolymer. Through the kinetic manipulation of charged, amphiphilic block copolymers in solution, we are able to generate different nanoscale structures with simple block copolymer chemistry. The technique relies on divalent organic counter ions and solvent mixtures to drive the organization of the block copolymers down specific pathways into complex one-dimensional structures. Block copolymers are increasingly used as templating materials; thus, the ability to control the formation of specific patterns and structures is of growing interest and applicability.
嵌段共聚物由两个或更多个通过共价键连接的化学性质不同的聚合物链段或嵌段组成。在溶液中,两亲性嵌段会由于链段之间的能量排斥作用而自组装。排斥程度、链段长度和溶剂选择性主要控制最终的组装形态。在理想情况下,人们希望能够在不改变嵌段共聚物化学性质的情况下改变形成的形态。通过对溶液中带电两亲性嵌段共聚物进行动力学操作,我们能够利用简单的嵌段共聚物化学方法生成不同的纳米级结构。该技术依靠二价有机抗衡离子和溶剂混合物来驱动嵌段共聚物沿着特定途径组织形成复杂的一维结构。嵌段共聚物越来越多地被用作模板材料;因此,控制特定图案和结构形成的能力越来越受到关注且具有实用性。