胶束
聚合
自组装
结晶
纳米技术
材料科学
构造(python库)
纳米尺度
化学
计算机科学
聚合物
复合材料
有机化学
水溶液
程序设计语言
作者
Jiaqian Nie,Jiantian Zhao,Lina Li,Tianyi Zhou,Gérald Guérin
出处
期刊:Angewandte Chemie
[Wiley]
日期:2025-08-04
卷期号:64 (39): e202511515-e202511515
被引量:4
标识
DOI:10.1002/anie.202511515
摘要
All the objects that surround us can be seen as combinations of elementary shapes like spheres, rods, and squares that perform complex tasks when connected in a well-defined manner. While making a device by assembling those shapes remains relatively easy at the human scale, it is extremely challenging to do so at the nanoscale, due to the difficulty to covalently attach at a defined position a nano-object with a given shape to another one of different geometry. To circumvent this hurdle, here, we introduce an innovative approach that consists in performing polymerization-induced self-assembly (PISA) onto core-crystalline micelles prepared by crystallization-driven self-assembly (CDSA). Because of the intrinsic properties of CDSA, one can construct one- or two-dimensional substrates to initiate PISA at very specific locations. Performing CDSA-substrated-PISA (CDSA-s-PISA) onto triblock co-micelles where only the central block was PISA active, led to the formation of elongated structures bearing one or two beads on their central parts, while CDSA-s-PISA on entirely PISA active micelles and in presence of free macro-CTA, allowed the preparation of uniform elongated micelles fully decorated with beads. These results offer a sneak peek of what the next generation of multitasks polymeric assemblies will be.
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