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超分子聚合物多态性形成过程中的单体与预成核簇

Monomers Versus Prenucleation Clusters En Route to Polymorphism of Supramolecular Polymers.

作者信息

Elizebath Drishya, Sharma Sanjay, Varughese Sunil, Ramachandran C N, Praveen Vakayil K

机构信息

Chemical Sciences and Technology Division, CSIR-National Institute for Interdisciplinary Science and Technology (CSIR-NIIST), Thiruvananthapuram, Kerala, 695019, India.

Academy of Scientific and Innovative Research (AcSIR), Ghaziabad, 201002, India.

出版信息

Small. 2025 Jan;21(1):e2405305. doi: 10.1002/smll.202405305. Epub 2024 Nov 3.

Abstract

Polymorphism in supramolecular polymers is strongly correlated with the polymerization pathways underlying their formation. To effectively control emerging polymorphs, a comprehensive understanding of nucleation pathways and mechanisms is essential. Herein, a coronene-dipeptide conjugate (Cr-o-FF) is introduced and its self-assembly into two different stable 1D supramolecular polymorphs (Agg 1 and 2f) is observed in the same solvent composition (water/THF, 7:3 v/v) and same concentration at room temperature, following two competitive self-assembly pathways. The difference in the mode of solvent addition triggers the two self-assembly pathways. Furthermore, the isolated intermediate Agg 2i is found to transform into Agg 1 or Agg 2f under controlled experimental conditions. The supramolecular aggregates of Cr-o-FF are thoroughly examined with the help of optical, chiroptical, and morphological techniques to understand the subtle difference in choosing the self-assembling pathways. The studies reveal that the nanotube formation of Agg 1 follows a classical nucleation-elongation supramolecular polymerization mechanism (involving monomers). In contrast, the helical fibers of Agg 2f are formed by the involvement of preorganized oligomers (nonclassical process). The observation highlights the underappreciated role of prenucleation clusters in pathway complexity and polymorphism of supramolecular 1D polymers.

摘要

超分子聚合物中的多态性与其形成过程中的聚合途径密切相关。为了有效控制新出现的多晶型物,全面了解成核途径和机制至关重要。在此,引入了一种并四苯 - 二肽共轭物(Cr - o - FF),在相同的溶剂组成(水/四氢呋喃,7:3 v/v)和相同浓度下,于室温下观察到其通过两种竞争性自组装途径自组装成两种不同的稳定一维超分子多晶型物(Agg 1和2f)。溶剂添加方式的差异触发了这两种自组装途径。此外,发现分离出的中间产物Agg 2i在可控的实验条件下可转化为Agg 1或Agg 2f。借助光学、手性光学和形态学技术对Cr - o - FF的超分子聚集体进行了全面研究,以了解选择自组装途径时的细微差异。研究表明,Agg 1的纳米管形成遵循经典的成核 - 伸长超分子聚合机制(涉及单体)。相比之下,Agg 2f的螺旋纤维是由预组装的低聚物参与形成的(非经典过程)。这一观察结果突出了预成核簇在超分子一维聚合物的途径复杂性和多态性中未被充分认识的作用。

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