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.
Langmuir. 2013 Jan 15;29(2):793-805. doi: 10.1021/la304957n. Epub 2013 Jan 4.
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) have been prepared. Careful analyses of correlations between the structures of these molecules and their gels have provided important insights into the factors responsible for one-dimensional aggregation of small molecules containing both lipophilic and hydrophilic parts. The gelation behavior has been examined in 30 liquids of diverse structure and polarity, and the properties of their gels and the gelation mechanisms have been investigated using a variety of techniques. Possible reasons are discussed regarding why the Pn are better gelators than the corresponding naphthyl analogues (Nn) which had been investigated previously. P2 and P3 are ambidextrous gelators (i.e., they gelate both water and some organic liquids), and P4-P8 gelate some organic liquids which are protic and aprotic, but not water. In at least one of the liquids examined, P3, P4, P6, P7, and P8 form gels at less than 1 w/v % concentrations, and some of the gels in 1-decanol are thixotropic. Analyses of the gelation abilities using Hansen solubility parameters yield both qualitative and quantitative insights into the role of liquid-gelator interactions. For example, the critical gelation concentrations increase generally with increasing polar and hydrogen bonding interactions between the gelators and their liquid components. As revealed by FT-IR, (1)H NMR, UV-vis, and fluorescence spectra, hydrogen-bonding between glucono units and π-π stacking between pyrenyl groups are important in the formation and maintenance of the gel networks. The results from this study, especially those relating the aggregation modes and liquid properties, offer insights for the design of new surfactant-containing low-molecular-mass gelators with predefined gelating abilities.
一系列含有 α,ω-二氨基烷烃间隔基的葡萄糖酸衍生的 1-芘磺酰基衍生物(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)已被制备。对这些分子的结构与其凝胶之间的相关性进行了仔细分析,为小分子一维聚集提供了重要的见解,这些小分子同时含有亲脂性和亲水性部分。在 30 种具有不同结构和极性的液体中研究了凝胶化行为,并使用各种技术研究了它们的凝胶性质和凝胶化机制。讨论了 Pn 比以前研究过的相应萘基类似物(Nn)更适合作为凝胶剂的可能原因。P2 和 P3 是双手性凝胶剂(即,它们凝胶化水和一些有机溶剂),而 P4-P8 凝胶化一些亲质子和非质子有机溶剂,但不凝胶化水。在至少一种研究的液体中,P3、P4、P6、P7 和 P8 在低于 1 w/v%的浓度下形成凝胶,并且 1-癸醇中的一些凝胶是触变的。使用 Hansen 溶解度参数分析凝胶化能力,为液体-凝胶剂相互作用提供了定性和定量的见解。例如,临界凝胶浓度通常随着凝胶剂与其液体成分之间的极性和氢键相互作用的增加而增加。如 FT-IR、(1)H NMR、UV-vis 和荧光光谱所示,葡萄糖单元之间的氢键和吡喃基之间的 π-π 堆积对于凝胶网络的形成和维持很重要。这项研究的结果,特别是与聚集模式和液体性质相关的结果,为设计具有预定凝胶能力的新型含表面活性剂的低分子量凝胶剂提供了见解。