单体与前核聚类对比 走向超分子聚合物的多态化
Drishya Elizebath1,2, Sanjay Sharma3, Sunil Varughese1,2
1Chemical Sciences and Technology Division, CSIR-National Institute for Interdisciplinary Science and Technology (CSIR-NIIST), Thiruvananthapuram, Kerala, 695019, India.
控制超分子聚合物多态性需要理解核化. 这项研究揭示了溶剂添加如何触发不同的自我组装途径,通过经典或非经典机制导致不同的多态.
科学领域:
- 超分子化学 超分子化学
- 聚合物科学 聚合物科学
- 材料科学 材料科学 材料科学
背景情况:
- 超分子聚合物的多态性与它们的形成途径有关.
- 控制多态体需要了解核化机制.
研究的目的:
- 为了研究一个冠二联 (Cr-o-FF OEt) 的自我组装到不同的1D超分子多态.
- 阐明核化路径和溶剂添加在指导自我组装中的作用.
- 区分经典和非经典的聚合机制.
主要方法:
- 一个冠二联的合成 (Cr-o-FF OEt).
- 控制的自组装实验不同溶剂添加模式.
- 使用光学,手术和形态技术进行表征.
- 对核和延长机制的分析.
主要成果:
- 在相同的溶剂组成和度下,从Cr-o-FFOEt中形成了两个稳定的1D超分子多态 (Agg 1和Agg 2f).
- 溶剂添加的模式被确定为竞争性自组装路径的触发因素.
- Agg 1通过经典的核化延长 (以单体为基础) 形成,而Agg 2f通过涉及预先组织的寡合体的非经典途径形成.
- 一种中间体 (Agg 2i) 被分离出来,并被证明可以转化为Agg 1或Agg 2f.
结论:
- 这项研究表明,在高分子聚合物中存在路径依赖的多态性.
- 溶剂添加模式极大地影响自我组装路径和由此产生的多态.
- 前核聚类在1D超分子聚合物中途径选择和多态性的复杂性中发挥着重要作用.
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