Cargando…
Preparation of Chiral Porous Organic Cage Clicked Chiral Stationary Phase for HPLC Enantioseparation
Porous organic cages (POCs) are a new subclass of porous materials, which are constructed from discrete cage molecules with permanent cavities via weak intermolecular forces. In this study, a novel chiral stationary phase (CSP) has been prepared by chemically binding a [4 + 6]-type chiral POC (C(120...
Autores principales: | , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10096354/ https://www.ncbi.nlm.nih.gov/pubmed/37049997 http://dx.doi.org/10.3390/molecules28073235 |
_version_ | 1785024316728934400 |
---|---|
author | Gong, Ya-Nan Ma, Qi-Yu Wang, Ying Zhang, Jun-Hui Zhang, You-Ping Liang, Rui-Xue Wang, Bang-Jin Xie, Sheng-Ming Yuan, Li-Ming |
author_facet | Gong, Ya-Nan Ma, Qi-Yu Wang, Ying Zhang, Jun-Hui Zhang, You-Ping Liang, Rui-Xue Wang, Bang-Jin Xie, Sheng-Ming Yuan, Li-Ming |
author_sort | Gong, Ya-Nan |
collection | PubMed |
description | Porous organic cages (POCs) are a new subclass of porous materials, which are constructed from discrete cage molecules with permanent cavities via weak intermolecular forces. In this study, a novel chiral stationary phase (CSP) has been prepared by chemically binding a [4 + 6]-type chiral POC (C(120)H(96)N(12)O(4)) with thiol-functionalized silica gel using a thiol-ene click reaction and applied to HPLC separations. The column packed with this CSP presented good separation capability for chiral compounds and positional isomers. Thirteen racemates have been enantioseparated on this column, including alcohols, diols, ketones, amines, epoxides, and organic acids. Upon comparison with a previously reported chiral POC NC1-R-based column, commercial Chiralpak AD-H, and Chiralcel OD-H columns, this column is complementary to these three columns in terms of its enantiomeric separation; and can also separate some racemic compounds that cannot be separated by the three columns. In addition, eight positional isomers (iodoaniline, bromoaniline, chloroaniline, dibromobenzene, dichlorobenzene, toluidine, nitrobromobenzene, and nitroaniline) have also been separated. The influences of the injection weight and column temperature on separation have been explored. After the column has undergone multiple injections, the relative standard deviations (RSDs) for the retention time and selectivity were below 1.0 and 1.5%, respectively, indicating the good reproducibility and stability of the column for separation. This work demonstrates that POCs are promising materials for HPLC separation. |
format | Online Article Text |
id | pubmed-10096354 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-100963542023-04-13 Preparation of Chiral Porous Organic Cage Clicked Chiral Stationary Phase for HPLC Enantioseparation Gong, Ya-Nan Ma, Qi-Yu Wang, Ying Zhang, Jun-Hui Zhang, You-Ping Liang, Rui-Xue Wang, Bang-Jin Xie, Sheng-Ming Yuan, Li-Ming Molecules Article Porous organic cages (POCs) are a new subclass of porous materials, which are constructed from discrete cage molecules with permanent cavities via weak intermolecular forces. In this study, a novel chiral stationary phase (CSP) has been prepared by chemically binding a [4 + 6]-type chiral POC (C(120)H(96)N(12)O(4)) with thiol-functionalized silica gel using a thiol-ene click reaction and applied to HPLC separations. The column packed with this CSP presented good separation capability for chiral compounds and positional isomers. Thirteen racemates have been enantioseparated on this column, including alcohols, diols, ketones, amines, epoxides, and organic acids. Upon comparison with a previously reported chiral POC NC1-R-based column, commercial Chiralpak AD-H, and Chiralcel OD-H columns, this column is complementary to these three columns in terms of its enantiomeric separation; and can also separate some racemic compounds that cannot be separated by the three columns. In addition, eight positional isomers (iodoaniline, bromoaniline, chloroaniline, dibromobenzene, dichlorobenzene, toluidine, nitrobromobenzene, and nitroaniline) have also been separated. The influences of the injection weight and column temperature on separation have been explored. After the column has undergone multiple injections, the relative standard deviations (RSDs) for the retention time and selectivity were below 1.0 and 1.5%, respectively, indicating the good reproducibility and stability of the column for separation. This work demonstrates that POCs are promising materials for HPLC separation. MDPI 2023-04-04 /pmc/articles/PMC10096354/ /pubmed/37049997 http://dx.doi.org/10.3390/molecules28073235 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Gong, Ya-Nan Ma, Qi-Yu Wang, Ying Zhang, Jun-Hui Zhang, You-Ping Liang, Rui-Xue Wang, Bang-Jin Xie, Sheng-Ming Yuan, Li-Ming Preparation of Chiral Porous Organic Cage Clicked Chiral Stationary Phase for HPLC Enantioseparation |
title | Preparation of Chiral Porous Organic Cage Clicked Chiral Stationary Phase for HPLC Enantioseparation |
title_full | Preparation of Chiral Porous Organic Cage Clicked Chiral Stationary Phase for HPLC Enantioseparation |
title_fullStr | Preparation of Chiral Porous Organic Cage Clicked Chiral Stationary Phase for HPLC Enantioseparation |
title_full_unstemmed | Preparation of Chiral Porous Organic Cage Clicked Chiral Stationary Phase for HPLC Enantioseparation |
title_short | Preparation of Chiral Porous Organic Cage Clicked Chiral Stationary Phase for HPLC Enantioseparation |
title_sort | preparation of chiral porous organic cage clicked chiral stationary phase for hplc enantioseparation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10096354/ https://www.ncbi.nlm.nih.gov/pubmed/37049997 http://dx.doi.org/10.3390/molecules28073235 |
work_keys_str_mv | AT gongyanan preparationofchiralporousorganiccageclickedchiralstationaryphaseforhplcenantioseparation AT maqiyu preparationofchiralporousorganiccageclickedchiralstationaryphaseforhplcenantioseparation AT wangying preparationofchiralporousorganiccageclickedchiralstationaryphaseforhplcenantioseparation AT zhangjunhui preparationofchiralporousorganiccageclickedchiralstationaryphaseforhplcenantioseparation AT zhangyouping preparationofchiralporousorganiccageclickedchiralstationaryphaseforhplcenantioseparation AT liangruixue preparationofchiralporousorganiccageclickedchiralstationaryphaseforhplcenantioseparation AT wangbangjin preparationofchiralporousorganiccageclickedchiralstationaryphaseforhplcenantioseparation AT xieshengming preparationofchiralporousorganiccageclickedchiralstationaryphaseforhplcenantioseparation AT yuanliming preparationofchiralporousorganiccageclickedchiralstationaryphaseforhplcenantioseparation |