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Guest-induced amorphous-to-crystalline transformation enables sorting of haloalkane isomers with near-perfect selectivity
The separation of haloalkane isomers with distillation-free strategies is one of the most challenging research topics in fundamental research and also gave high guiding values to practical industrial applications. Here, this contribution provides a previously unidentified solid supramolecular adsorp...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Association for the Advancement of Science
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9166396/ https://www.ncbi.nlm.nih.gov/pubmed/35658045 http://dx.doi.org/10.1126/sciadv.abo2255 |
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author | Wu, Jia-Rui Wu, Gengxin Li, Dongxia Dai, Dihua Yang, Ying-Wei |
author_facet | Wu, Jia-Rui Wu, Gengxin Li, Dongxia Dai, Dihua Yang, Ying-Wei |
author_sort | Wu, Jia-Rui |
collection | PubMed |
description | The separation of haloalkane isomers with distillation-free strategies is one of the most challenging research topics in fundamental research and also gave high guiding values to practical industrial applications. Here, this contribution provides a previously unidentified solid supramolecular adsorption material based on a leggero pillararene derivative BrP[5]L, which can separate 1-/2-bromoalkane isomers with near-ideal selectivity. Activated solids of BrP[5]L with interesting amorphous and nonporous features could adsorb 1-bromopropane and 1-bromobutane from the corresponding equal volume mixtures of 1-/2-positional isomers with purities of 98.1 and 99.0%, respectively. Single-crystal structures incorporating theoretical calculation reveal that the high selectivity originates from the higher thermostability of 1-bromoalkane–loaded structures compared to its corresponding isomer-loaded structures, which could be further attributed to the perfect size/shape match between BrP[5]L and 1-bromoalkanes. Moreover, control experiments using its counterpart macrocycle of traditional pillararene demonstrate that BrP[5]L has better adsorptive selectivity, benefiting from the intrinsic free-rotation phenylene subunit on its backbone. |
format | Online Article Text |
id | pubmed-9166396 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Association for the Advancement of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-91663962022-06-17 Guest-induced amorphous-to-crystalline transformation enables sorting of haloalkane isomers with near-perfect selectivity Wu, Jia-Rui Wu, Gengxin Li, Dongxia Dai, Dihua Yang, Ying-Wei Sci Adv Physical and Materials Sciences The separation of haloalkane isomers with distillation-free strategies is one of the most challenging research topics in fundamental research and also gave high guiding values to practical industrial applications. Here, this contribution provides a previously unidentified solid supramolecular adsorption material based on a leggero pillararene derivative BrP[5]L, which can separate 1-/2-bromoalkane isomers with near-ideal selectivity. Activated solids of BrP[5]L with interesting amorphous and nonporous features could adsorb 1-bromopropane and 1-bromobutane from the corresponding equal volume mixtures of 1-/2-positional isomers with purities of 98.1 and 99.0%, respectively. Single-crystal structures incorporating theoretical calculation reveal that the high selectivity originates from the higher thermostability of 1-bromoalkane–loaded structures compared to its corresponding isomer-loaded structures, which could be further attributed to the perfect size/shape match between BrP[5]L and 1-bromoalkanes. Moreover, control experiments using its counterpart macrocycle of traditional pillararene demonstrate that BrP[5]L has better adsorptive selectivity, benefiting from the intrinsic free-rotation phenylene subunit on its backbone. American Association for the Advancement of Science 2022-06-03 /pmc/articles/PMC9166396/ /pubmed/35658045 http://dx.doi.org/10.1126/sciadv.abo2255 Text en Copyright © 2022 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (https://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited. |
spellingShingle | Physical and Materials Sciences Wu, Jia-Rui Wu, Gengxin Li, Dongxia Dai, Dihua Yang, Ying-Wei Guest-induced amorphous-to-crystalline transformation enables sorting of haloalkane isomers with near-perfect selectivity |
title | Guest-induced amorphous-to-crystalline transformation enables sorting of haloalkane isomers with near-perfect selectivity |
title_full | Guest-induced amorphous-to-crystalline transformation enables sorting of haloalkane isomers with near-perfect selectivity |
title_fullStr | Guest-induced amorphous-to-crystalline transformation enables sorting of haloalkane isomers with near-perfect selectivity |
title_full_unstemmed | Guest-induced amorphous-to-crystalline transformation enables sorting of haloalkane isomers with near-perfect selectivity |
title_short | Guest-induced amorphous-to-crystalline transformation enables sorting of haloalkane isomers with near-perfect selectivity |
title_sort | guest-induced amorphous-to-crystalline transformation enables sorting of haloalkane isomers with near-perfect selectivity |
topic | Physical and Materials Sciences |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9166396/ https://www.ncbi.nlm.nih.gov/pubmed/35658045 http://dx.doi.org/10.1126/sciadv.abo2255 |
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