Zhao Hongmeng, Xu Zhanwen, Lin Jiaping
Shanghai Key Laboratory of Advanced Polymeric Materials, Key Laboratory for Ultrafine Materials of Ministry of Education, Frontiers Science Center for Materiobiology and Dynamic Chemistry, School of Materials Science and Engineering, East China University of Science and Technology, Shanghai, 200237, China.
State Key Laboratory of Molecular Engineering of Polymers, Department of Macromolecular Science, Fudan University, Shanghai, 200438, China.
Macromol Rapid Commun. 2022 May;43(9):e2100855. doi: 10.1002/marc.202100855. Epub 2022 Mar 23.
Chiral nanostructures of nanoparticle assemblies have attracted tremendous interest for their fascinating functional properties. Herein, through theoretical simulations, it is shown that nanoparticle tethered block copolymers can self-assemble into hierarchically chiral nanostructures. Twofold helices are formed in the hierarchically chiral nanostructures: the diblock copolymers form helical supercylinders while the nanoparticles arrange into chiral assemblies wrapped around the helical supercylinders. The hierarchically chiral nanostructures can be formed in a large parameter window. Circular dichroism calculations demonstrate that the coexistence of polymeric helices and chiral nanoparticle assemblies improves the chiroptical activity. These findings can provide guidelines for designing hierarchically ordered chiral nanostructures with advanced functional properties.
纳米颗粒组装体的手性纳米结构因其迷人的功能特性而引起了极大的兴趣。在此,通过理论模拟表明,纳米颗粒连接的嵌段共聚物可以自组装成具有分级手性的纳米结构。在分级手性纳米结构中形成了双螺旋结构:二嵌段共聚物形成螺旋超圆柱体,而纳米颗粒排列成包裹在螺旋超圆柱体周围的手性组装体。分级手性纳米结构可以在较大的参数窗口内形成。圆二色性计算表明,聚合物螺旋和手性纳米颗粒组装体的共存提高了手性光学活性。这些发现可为设计具有先进功能特性的分级有序手性纳米结构提供指导。