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首页> 外文期刊>Helvetica chimica acta >Supramolecular Hydrogels Based on L-Phenylalanine Derivatives with a Positively Charged Terminal Group
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Supramolecular Hydrogels Based on L-Phenylalanine Derivatives with a Positively Charged Terminal Group

机译:基于带有正电荷端基的L-苯丙氨酸衍生物的超分子水凝胶

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摘要

A new hydrogelator based on L-phenylalanine with a long hydrophobic chain and positively charged terminus was synthesized, and its gelation behavior in H2O was investigated. Polarized optical microscopy (POM), field emission scanning electron microscopy (FE-SEM). and X-ray diffraction (XRD) results indicate that the hydrogelator self-assembles into fibres-like aggregates which then lead to the formation of a hydrogel. H-1-NMR and CD spectra of hydrogels and aqueous solution revealed that intermolecular H-bonding between the amide groups was the driving force for gelation. A luminescence in which ANS (8-anilinonaphthalene-1-sulfonic acid) was used as a probe, indicated that the hydrophobic interactions between long chains were the driving force for gelation. Consequently, it was proved that the hydrogelator self-assembles into fibre-like agggregates and then forms supramolecular hydrogels through the H-bonding and hydrophobic interactions.
机译:合成了一种基于L-苯丙氨酸,具有长疏水链和带正电荷末端的新型水凝胶剂,并研究了其在水中的胶凝行为。偏光光学显微镜(POM),场发射扫描电子显微镜(FE-SEM)。 X射线衍射(XRD)结果表明,水凝胶化剂自组装成纤维状聚集体,然后导致形成水凝胶。水凝胶和水溶液的H-1-NMR和CD光谱表明,酰胺基之间的分子间H键是凝胶化的驱动力。以ANS(8-苯胺基萘-1-磺酸)为探针的发光表明长链之间的疏水相互作用是凝胶化的驱动力。因此,证明了水凝胶化剂自组装成纤维状聚集体,然后通过H键和疏水相互作用形成超分子水凝胶。

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