Zofchak Everett S, LaNasa Jacob A, Mei Wenwen, Hickey Robert J
ACS Macro Lett. 2018 Jul 17;7(7):822-827. doi: 10.1021/acsmacrolett.8b00378. Epub 2018 Jun 22.
Polymerization-induced structural transitions have gained attention recently due to the ease of creating and modifying nanostructured materials with controlled morphologies and length scales. Here, we show that order-order and disorder-order nanostructural transitions are possible using in situ polymer grafting from the diblock polymer, poly(styrene)--poly(butadiene). In our approach, we are able to control the resulting nanostructure (lamellar, hexagonally packed cylinders, and disordered spheres) by changing the initial block polymer/monomer ratio. The nanostructural transition occurs by a grafting from mechanism in which poly(styrene) chains are initiated from the poly(butadiene) block via the creation of an allylic radical, which increases the overall molecular weight and the poly(styrene) volume fraction. The work presented here highlights how the chemical process of converting standard linear diblock copolymers to grafted block polymers drives interesting and controllable polymerization-induced morphology transitions.
由于能够轻松制备和修饰具有可控形态和长度尺度的纳米结构材料,聚合诱导的结构转变最近受到了关注。在此,我们表明,通过从二嵌段聚合物聚(苯乙烯)-聚(丁二烯)进行原位聚合物接枝,可以实现有序-有序和无序-有序的纳米结构转变。在我们的方法中,我们能够通过改变初始嵌段聚合物/单体比例来控制所得的纳米结构(层状、六方堆积圆柱状和无序球状)。纳米结构转变通过接枝机理发生,其中聚(苯乙烯)链通过烯丙基自由基的产生从聚(丁二烯)嵌段引发,这增加了总分子量和聚(苯乙烯)体积分数。本文介绍的工作突出了将标准线性二嵌段共聚物转化为接枝嵌段聚合物的化学过程如何驱动有趣且可控的聚合诱导形态转变。