首页> 外文期刊>Langmuir: The ACS Journal of Surfaces and Colloids >Organogelation and Hydrogelation of Low-Molecular-Weight Amphiphilic Dipeptides: pH Responsiveness in Phase-Selective Gelation and Dye Removal
【24h】

Organogelation and Hydrogelation of Low-Molecular-Weight Amphiphilic Dipeptides: pH Responsiveness in Phase-Selective Gelation and Dye Removal

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

获取原文
获取原文并翻译 | 示例
           

摘要

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 wits employed in the instant removal of large amounts of dyes for wastewater treatment.
机译:寻找具有可能的结构活性相关性的高效低分子量胶凝剂(LMWG)的趋势正在上升。本工作报告了一套新型的两亲二肽基羧酸,能够有效地胶凝有机溶剂。更有趣的是,它们的钠盐在有机凝胶化方面表现出增强的效率,并具有使水凝胶化的附加能力。存在于两亲性二肽的羧酸钠的聚集体中的静电相互作用似乎很重要,因为某些非胶凝剂羧酸在形成盐时被证明是极好的胶凝剂。系统地更改了二肽部分中氨基酸的组合和顺序,以了解氨基酸的非极性脂族/芳族取代在两亲物自组装行为中的集体重要性。在逆转氨基酸残基的序列时,观察到胶凝能力几乎提高了20倍,并且在某些情况下,非胶凝剂转化为有效的胶凝剂。这些热可逆有机/水凝胶的光谱和显微镜研究表明,非共价相互作用的平衡参与,包括氢键和。范德华相互作用对于有机/水凝胶化至关重要。这些二肽从其与水的混合物中选择性地使有机溶剂胶凝,并且由这些有机凝胶制备的干凝胶显示出染料(如结晶紫)的时间依赖性吸附。这些胶凝剂的最显着特征是pH响应性,该响应性可用于油和水的双相混合物中任一溶剂的pH依赖性相选择性胶凝。酸和盐的不同的凝胶化能力是由于在立即去除大量染料以进行废水处理时所用的两亲性二肽机体的pH响应性引起的。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号