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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...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2020
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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. |
format | Online Article Text |
id | pubmed-9057107 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
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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