超分子化学
紧身衣
氢键
两亲性
水溶液
聚合物
共价键
材料科学
超分子聚合物
自组装
纳米结构
超分子组装
纳米线
卟啉
化学工程
化学
高分子化学
纳米技术
共聚物
分子
有机化学
荧光
物理
工程类
量子力学
作者
Liangliang Zhou,Jiayi Chen,Lanying Li,Hang Li,Huan Wang,De‐Gao Wang,Gui‐Chao Kuang
标识
DOI:10.1002/marc.201900182
摘要
Abstract The aggregate morphologies of 4,4‐difluoro‐4‐bora‐3a,4a‐diaza‐ s ‐indacene (BODIPY) main chain supramolecular polymer amphiphiles (SPA) are tunable by a fine balance of different non‐covalent interactions. When the BODIPY segments and sodium cholate are mixed in aqueous solution, they form SPA by electrostatic attraction and hydrogen‐bonds. This SPA displays helical nanowires' morphology. After the third component dimeric β‐cyclodextrin (β‐CD‐C) is added, the hydrogen bonds between the cholate are substituted by the host–guest interaction between cholate and β‐CD‐C. Therefore, these SPA transform their aggregate morphologies into nanosheets' architecture. Therefore, a simple and effective way to regulate self‐assembly by non‐covalent forces is developed. This supramolecular method may provide an effective way to prepare various nanostructures in aqueous solution and show promising application in the future.
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