Key Laboratory of Applied Surface and Colloid Chemistry (Ministry of Education), School of Chemistry and Chemical Engineering, Shaanxi Normal University, Xi'an 710062, P. R. China.
J Am Chem Soc. 2013 Jun 19;135(24):8989-99. doi: 10.1021/ja402560n. Epub 2013 Jun 4.
The self-assembly behavior of a series of glucono-appended 1-pyrenesulfonyl derivatives containing α,ω-diaminoalkane spacers (Pn, where n, the number of methylene units separating the amino groups, is 2, 3, 4, 6, 7, and 8) in v:v tetrahydrofuran (THF):water mixtures is examined at room temperature. The Pn at 2 w/v % concentrations do not dissolve in either THF or water at room temperature. However, the Pn can be dissolved in some THF:water mixtures, and they form gels spontaneously in other compositions without dissolving completely. The self-assembly of the Pn in the liquid mixtures has been investigated using a variety of techniques. The particle sizes of the Pn in their solutions/sols, critical gelation concentrations, microstructures, thermal and mechanical stabilities of the gels, and molecular packing modes of Pn molecules in their gel networks are found to be very dependent on the composition of the liquid mixtures. Correlations between the self-assembly behavior of the Pn and the polarity of the liquid mixtures, as probed by E(T)(30) and Hansen solubility parameters, yield both qualitative and quantitative insights into why self-assembly of the Pn can or cannot be achieved in different liquid compositions. As revealed by UV-vis and fluorescence spectroscopy studies, π-π stacking of the pyrenyl groups occurs as part of the aggregation process. Correlations between the rheological properties of the gels and the Hansen solubility parameters of the Pn and the solvent mixtures indicate that hydrogen-bonding interactions are a major contributor to the mechanical stability. Overall, the results of this study offer a new strategy to investigate the balance between dissolution and aggregation of molecular gelators. To the best of our knowledge, this is the first example of the spontaneous formation of molecular gels without heating by placing gelators in mixtures of liquids in which they are insoluble in the neat components.
在室温下,考察了一系列含有α,ω-二氨基烷间隔基的葡萄糖基 appended 1-苯磺酰基衍生物(Pn,其中 n 是氨基之间的亚甲基单元数,分别为 2、3、4、6、7 和 8)在 v:v 四氢呋喃(THF):水混合物中的自组装行为。在室温下,Pn 在 2 w/v%浓度下既不溶于 THF 也不溶于水。然而,Pn 可以溶解在一些 THF:水混合物中,并且在其他组成下它们会自发形成凝胶而不完全溶解。使用各种技术研究了 Pn 在液体混合物中的自组装。Pn 在其溶液/溶胶中的颗粒大小、临界凝胶浓度、微观结构、凝胶的热和机械稳定性以及 Pn 分子在其凝胶网络中的分子堆积模式都非常依赖于液体混合物的组成。通过 E(T)(30)和 Hansen 溶解度参数研究 Pn 的自组装行为与液体混合物极性之间的相关性,为为什么 Pn 的自组装可以或不能在不同的液体组成中实现提供了定性和定量的见解。通过紫外可见和荧光光谱研究揭示,苯并吡喃基的π-π 堆积发生在聚集过程的一部分。凝胶的流变性质与 Pn 和溶剂混合物的 Hansen 溶解度参数之间的相关性表明氢键相互作用是机械稳定性的主要贡献者。总的来说,这项研究的结果提供了一种新的策略来研究分子凝胶剂的溶解和聚集之间的平衡。据我们所知,这是第一个将凝胶剂置于它们在纯组分中不溶的液体混合物中而无需加热即可自发形成分子凝胶的例子。