Yu Xiaoliang, Fang Yuanjian, Luo Zhiruo, Guo Xingjian, Fu Lulu, Fan Zhi, Zhao Jin, Xie Hongxiang, Guo Minjie, Cheng Bowen
Tianjin Key Laboratory of Brine Chemical Engineering and Resource Eco-utilization, College of Chemical Engineering and Materials Science, Tianjin University of Science & Technology, Tianjin 300457, P. R. China.
State Key Laboratory of Biobased Fiber Manufacturing Technology, Tianjin University of Science & Technology, Tianjin 300457, P. R. China.
J Am Chem Soc. 2025 Jan 15;147(2):2193-2205. doi: 10.1021/jacs.4c16546. Epub 2025 Jan 3.
Polymer nanoparticles with low curvature, especially two-dimensional (2D) soft materials, are rich in functions and outstanding properties and have received extensive attention. Crystallization-driven self-assembly (CDSA) of linear semicrystalline block copolymers is currently a common method of constructing 2D platelets of uniform size. Although accompanied by high controllability, this CDSA method usually and inevitably requires a longer aging time and lower assembly concentration, limiting the large-scale preparation of nanoaggregates. In this study, a series of all-bottlebrush-type block copolymers, poly(octadecyl acrylate)--poly(oligoethylene glycol methyl ether methacrylate)s are prepared by living polymerization. Driven by the synergistic crystallization of crystalline side chains and the rapid microphase separation of bottlebrush topology, these polymers can assemble into uniform 2D circular platelet micelles in a few minutes, without being affected by a high assembly concentration. In this process, epitaxial growth of the bottlebrush molecules proceeds with rigid cylindrical molecular conformation at the micelle crystallization sites and eventually provides a sandwich-type micelle according to a head-to-head stacking mode. This is explained as a "crystallization-assisted rapid microphase separation" mechanism. The micelle structures are affected by the assembly solvent and temperature, the size of which shows a linear dependence on the assembly temperature below the melting point of the crystalline block, which can be used to precisely control the morphology of these 2D platelets. This study establishes an efficient and rapid method to prepare 2D polymer nanosoft materials, which are promising candidates for further development, preparation, and application of various nanomaterials.
具有低曲率的聚合物纳米颗粒,特别是二维(2D)软材料,功能丰富且性能优异,受到了广泛关注。线性半结晶嵌段共聚物的结晶驱动自组装(CDSA)是目前构建尺寸均匀的二维片晶的常用方法。尽管具有高度可控性,但这种CDSA方法通常不可避免地需要更长的老化时间和更低的组装浓度,限制了纳米聚集体的大规模制备。在本研究中,通过活性聚合制备了一系列全刷型嵌段共聚物,聚(丙烯酸十八烷基酯)-聚(聚乙二醇甲基醚甲基丙烯酸酯)。在结晶侧链的协同结晶和刷状拓扑结构的快速微相分离的驱动下,这些聚合物可以在几分钟内组装成均匀的二维圆形片状胶束,而不受高组装浓度的影响。在此过程中,刷状分子在胶束结晶位点以刚性圆柱状分子构象进行外延生长,最终根据头对头堆积模式提供三明治型胶束。这被解释为一种“结晶辅助快速微相分离”机制。胶束结构受组装溶剂和温度的影响,其尺寸在低于结晶嵌段熔点的组装温度下呈线性依赖关系,可用于精确控制这些二维片晶的形态。本研究建立了一种高效快速的方法来制备二维聚合物纳米软材料,这些材料有望进一步用于各种纳米材料的开发、制备和应用。