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首页> 外文期刊>RSC Advances >One-step-synthesized d-gluconic acetal-based supramolecular organogelators with effective phase-selective gelation
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One-step-synthesized d-gluconic acetal-based supramolecular organogelators with effective phase-selective gelation

机译:基于一步合成的D-葡萄糖缩缩的超分子器官,具有有效相选择性凝胶化

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摘要

Two effective and one-step-synthesized organogelators based on D -gluconic acetal derivatives have been developed to show phase-selective gelation behaviours towards aromatic solvents from their biphasic mixtures with water. The dominant factors that drive gelation have been studied using FT-IR and temperature-dependent ~(1) H NMR spectroscopy. Particularly, gelator GAA-2 in powder form could selectively congeal toluene, benzene and o -xylene at room temperature under mild stirring. Additionally, GAA-2 could gelate the aromatic solvents within 10 min and the recovery rate of the aromatic solvents could reach about 82% under a certain condition. The benefits of wide source availability, being easy to synthesize, and recyclable performance of the gelator make GAA-2 ideal for real-world remediation of aromatic solvents.
机译:已经开发了基于D戊酰基缩醛衍生物的两步和一步合成的有机凝胶蛋白,以显示与水的双相混合物朝向芳族溶剂的相位选择性凝胶化行为。使用FT-IR和温度依赖性〜(1)H NMR光谱研究了驱动凝胶化的主要因素。特别地,在温和搅拌下,粉末形式的墨水GaA-2可以在室温下选择性地凝集甲苯,苯和o - 苯乙烯。另外,GaA-2可以在10分钟内凝聚芳族溶剂,并且在一定条件下芳族溶剂的回收率可达到约82%。广泛源可用性的好处,易于合成,凝胶胶的可回收性能使GaA-2成为真实溶血溶剂的真实修复的理想选择。

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