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低分子量两亲性二肽的凝胶化和水凝胶化:相选择性凝胶化和染料去除中的 pH 响应性。

Organogelation and hydrogelation of low-molecular-weight amphiphilic dipeptides: pH responsiveness in phase-selective gelation and dye removal.

机构信息

Department of Biological Chemistry, Indian Association for the Cultivation of Science Jadavpur, Kolkata - 700 032, India.

出版信息

Langmuir. 2009 Aug 4;25(15):8639-48. doi: 10.1021/la804235e.

Abstract

The search for efficient low-molecular-weight gelators (LMWGs) with possible structure-activity correlation is on the rise. The present work reports a novel set of amphiphilic dipeptide-based carboxylic acids capable of efficiently gelating organic solvents. More interestingly, their sodium salts showed enhanced efficiency in organogelation with the additional ability to gelate water. Electrostatic interactions present in the aggregation of the sodium carboxylates of amphiphilic dipeptides seem to be important because some of the nongelator carboxylic acids turned out to be excellent gelators upon salt formation. The combinations and sequence of the amino acids in the dipeptide moiety were systematically altered to understand the collective importance of the nonpolar aliphatic/aromatic substitution in amino acids in the self-assembling behavior of amphiphiles. Almost a 20-fold enhancement in the gelation ability was observed on reversing the sequence of the amino acid residues, and in some cases, nongelators were transformed to efficient gelators. Spectroscopic and microscopic studies of these thermoreversible organo/hydrogels revealed that balanced participation of the noncovalent interactions including hydrogen bonding and van der Waals interactions are crucial for organo/hydrogelation. These dipeptides selectively gelate organic solvents from their mixtures with water, and the xerogels prepared from these organogels showed time-dependent adsorption of dyes such as crystal violet. The most remarkable feature of these gelators is the pH responsiveness, which was aptly utilized for the pH-dependent phase-selective gelation of either solvent in a biphasic mixture of oil and water. The dissimilar gelation ability of the acid and its salt originating from the pH responsiveness of the amphiphilic dipeptide was employed in the instant removal of large amounts of dyes for wastewater treatment.

摘要

寻找具有可能的结构-活性相关性的高效低分子量凝胶剂(LMWG)的研究正在兴起。本工作报道了一组新型两亲性二肽基羧酸,它们能够有效地凝胶有机溶剂。更有趣的是,它们的钠盐在凝胶化有机相方面表现出更高的效率,并且具有凝胶化水的额外能力。在两亲性二肽羧酸的聚集中存在的静电相互作用似乎很重要,因为一些非凝胶形成羧酸在形成盐后变成了极好的凝胶形成剂。系统地改变二肽部分中的氨基酸的组合和序列,以了解非极性脂肪族/芳族取代氨基酸在两亲体自组装行为中的集体重要性。在氨基酸残基的序列反转时,凝胶形成能力几乎增强了 20 倍,在某些情况下,非凝胶形成剂转变为高效凝胶形成剂。这些热可逆有机/水凝胶的光谱和显微镜研究表明,包括氢键和范德华相互作用在内的非共价相互作用的平衡参与对于有机/水凝胶化至关重要。这些二肽选择性地从其与水的混合物中凝胶化有机溶剂,并且从这些有机凝胶制备的干凝胶显示出对染料(例如结晶紫)的时间依赖性吸附。这些凝胶剂的最显著特征是 pH 响应性,该特征可用于在油和水的两相混合物中的溶剂的 pH 依赖性相选择性凝胶化。两亲性二肽的 pH 响应性导致酸及其盐的不同凝胶形成能力被用于即时去除废水中的大量染料以进行废水处理。

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