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Selective adsorptive separation of cyclohexane over benzene using thienothiophene cages
The selective separation of benzene (Bz) and cyclohexane (Cy) is one of the most challenging chemical separations in the petrochemical and oil industries. In this work, we report an environmentally friendly and energy saving approach to separate Cy over Bz using thienothiophene cages (ThT-cages) wit...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8179544/ https://www.ncbi.nlm.nih.gov/pubmed/34163764 http://dx.doi.org/10.1039/d1sc00440a |
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author | Ding, Yanjun Alimi, Lukman O. Moosa, Basem Maaliki, Carine Jacquemin, Johan Huang, Feihe Khashab, Niveen M. |
author_facet | Ding, Yanjun Alimi, Lukman O. Moosa, Basem Maaliki, Carine Jacquemin, Johan Huang, Feihe Khashab, Niveen M. |
author_sort | Ding, Yanjun |
collection | PubMed |
description | The selective separation of benzene (Bz) and cyclohexane (Cy) is one of the most challenging chemical separations in the petrochemical and oil industries. In this work, we report an environmentally friendly and energy saving approach to separate Cy over Bz using thienothiophene cages (ThT-cages) with adaptive porosity. Interestingly, cyclohexane was readily captured selectively from an equimolar benzene/cyclohexane mixture with a purity of 94%. This high selectivity arises from the C–H⋯S, C–H⋯π and C–H⋯N interactions between Cy and the thienothiophene ligand. Reversible transformation between the nonporous guest-free structure and the host–guest assembly, endows this system with excellent recyclability with minimal energy requirements. |
format | Online Article Text |
id | pubmed-8179544 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-81795442021-06-22 Selective adsorptive separation of cyclohexane over benzene using thienothiophene cages Ding, Yanjun Alimi, Lukman O. Moosa, Basem Maaliki, Carine Jacquemin, Johan Huang, Feihe Khashab, Niveen M. Chem Sci Chemistry The selective separation of benzene (Bz) and cyclohexane (Cy) is one of the most challenging chemical separations in the petrochemical and oil industries. In this work, we report an environmentally friendly and energy saving approach to separate Cy over Bz using thienothiophene cages (ThT-cages) with adaptive porosity. Interestingly, cyclohexane was readily captured selectively from an equimolar benzene/cyclohexane mixture with a purity of 94%. This high selectivity arises from the C–H⋯S, C–H⋯π and C–H⋯N interactions between Cy and the thienothiophene ligand. Reversible transformation between the nonporous guest-free structure and the host–guest assembly, endows this system with excellent recyclability with minimal energy requirements. The Royal Society of Chemistry 2021-02-25 /pmc/articles/PMC8179544/ /pubmed/34163764 http://dx.doi.org/10.1039/d1sc00440a Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/ |
spellingShingle | Chemistry Ding, Yanjun Alimi, Lukman O. Moosa, Basem Maaliki, Carine Jacquemin, Johan Huang, Feihe Khashab, Niveen M. Selective adsorptive separation of cyclohexane over benzene using thienothiophene cages |
title | Selective adsorptive separation of cyclohexane over benzene using thienothiophene cages |
title_full | Selective adsorptive separation of cyclohexane over benzene using thienothiophene cages |
title_fullStr | Selective adsorptive separation of cyclohexane over benzene using thienothiophene cages |
title_full_unstemmed | Selective adsorptive separation of cyclohexane over benzene using thienothiophene cages |
title_short | Selective adsorptive separation of cyclohexane over benzene using thienothiophene cages |
title_sort | selective adsorptive separation of cyclohexane over benzene using thienothiophene cages |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8179544/ https://www.ncbi.nlm.nih.gov/pubmed/34163764 http://dx.doi.org/10.1039/d1sc00440a |
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