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One-step-synthesized d-gluconic acetal-based supramolecular organogelators with effective phase-selective gelation

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 t...

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Autores principales: Fan, Kaiqi, Wang, Xiaobo, Wang, Xiao, Yang, Haoran, Han, Guanglu, Zhou, Liming, Fang, Shaoming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9057107/
https://www.ncbi.nlm.nih.gov/pubmed/35521241
http://dx.doi.org/10.1039/d0ra07658a
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author Fan, Kaiqi
Wang, Xiaobo
Wang, Xiao
Yang, Haoran
Han, Guanglu
Zhou, Liming
Fang, Shaoming
author_facet Fan, Kaiqi
Wang, Xiaobo
Wang, Xiao
Yang, Haoran
Han, Guanglu
Zhou, Liming
Fang, Shaoming
author_sort Fan, Kaiqi
collection PubMed
description 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.
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spelling pubmed-90571072022-05-04 One-step-synthesized d-gluconic acetal-based supramolecular organogelators with effective phase-selective gelation Fan, Kaiqi Wang, Xiaobo Wang, Xiao Yang, Haoran Han, Guanglu Zhou, Liming Fang, Shaoming RSC Adv Chemistry 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. The Royal Society of Chemistry 2020-10-08 /pmc/articles/PMC9057107/ /pubmed/35521241 http://dx.doi.org/10.1039/d0ra07658a Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Fan, Kaiqi
Wang, Xiaobo
Wang, Xiao
Yang, Haoran
Han, Guanglu
Zhou, Liming
Fang, Shaoming
One-step-synthesized d-gluconic acetal-based supramolecular organogelators with effective phase-selective gelation
title One-step-synthesized d-gluconic acetal-based supramolecular organogelators with effective phase-selective gelation
title_full One-step-synthesized d-gluconic acetal-based supramolecular organogelators with effective phase-selective gelation
title_fullStr One-step-synthesized d-gluconic acetal-based supramolecular organogelators with effective phase-selective gelation
title_full_unstemmed One-step-synthesized d-gluconic acetal-based supramolecular organogelators with effective phase-selective gelation
title_short One-step-synthesized d-gluconic acetal-based supramolecular organogelators with effective phase-selective gelation
title_sort one-step-synthesized d-gluconic acetal-based supramolecular organogelators with effective phase-selective gelation
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9057107/
https://www.ncbi.nlm.nih.gov/pubmed/35521241
http://dx.doi.org/10.1039/d0ra07658a
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