Supramolecular Polymerization of all- cis -Fluorinated Cyclohexanes: Influence of Side Chains

S. V. Haridas, Oleksandr Shyshov, Max von Delius
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Abstract

Custom-designed materials based on supramolecular polymers are of interest for applications in organic electronics and biomedicine. Recently, we have shown that derivatives of the highly polar compound all-cis hexafluorocyclohexane undergo seeded polymerization and can therefore be used to prepare soluble nanofibers with controlled length. In this work, we aimed to explore the scope of this process. We studied the supramolecular polymerization of six all-cis-fluorinated cyclohexane monomers, with five differing in the solubilizing side chains and one in the secondary supramolecular binding site. In studies on controlled supramolecular polymerization, we found that three of the monomers could be induced to polymerize by ultrasound irradiation and four by addition of seeds. For these latter examples, we were able to identify a solvent mixture that led to spontaneous polymerization and hysteresis in heating and cooling curves. These results show that the living supramolecular polymerization of fluorinated cyclohexanes is not limited to one particular monomer, but that side chains exhibiting a strong solvophobic effect that cannot be compensated within the binary solvent “window” represent a limitation to the approach. We also demonstrate that nanofibers based on stacks of fluorinated cyclohexanes can be dissociated by addition of chloride ions.

Abstract Image

全顺氟环己烷的超分子聚合反应:侧链的影响
基于超分子聚合物的定制设计材料在有机电子和生物医学领域的应用很有兴趣。最近,我们已经证明了高极性化合物全顺式六氟环己烷的衍生物经过种子聚合,因此可以用来制备长度可控的可溶性纳米纤维。在这项工作中,我们旨在探索这一过程的范围。我们研究了六个全顺式氟化环己烷单体的超分子聚合,其中五个在增溶侧链上不同,一个在二级超分子结合位点上不同。在可控超分子聚合的研究中,我们发现其中3个单体可以通过超声照射诱导聚合,4个单体可以通过添加种子诱导聚合。对于后一个例子,我们能够确定溶剂混合物,导致自发聚合和滞后的加热和冷却曲线。这些结果表明,氟化环己烷的活性超分子聚合并不局限于一种特定的单体,但表现出强烈的疏溶剂效应的侧链不能在二元溶剂“窗口”内补偿,这是该方法的局限性。我们还证明了基于氟化环己烷堆叠的纳米纤维可以通过添加氯离子来解离。
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来源期刊
CiteScore
3.70
自引率
0.00%
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审稿时长
12 weeks
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