One‐step strategy for the synthesis of a derivatized cyclodextrin‐based monolithic column
Derivatized β‐cyclodextrin (β‐CD) functionalized monolithic columns were prepared by a “one‐step” strategy using click chemistry. First, the intended derivatized β‐CD monomers were synthesized by a click reaction between propargyl methacrylate and mono‐6‐azido‐β‐CD and then sulfonation or methylatio...
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Published in | Journal of separation science Vol. 37; no. 14; pp. 1720 - 1727 |
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Main Authors | , , , , , , |
Format | Journal Article Web Resource |
Language | English |
Published |
Weinheim
Wiley-VCH
01.07.2014
Blackwell Publishing Ltd Wiley Wiley Subscription Services, Inc |
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Online Access | Get full text |
ISSN | 1615-9306 1615-9314 1615-9314 |
DOI | 10.1002/jssc.201400312 |
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Abstract | Derivatized β‐cyclodextrin (β‐CD) functionalized monolithic columns were prepared by a “one‐step” strategy using click chemistry. First, the intended derivatized β‐CD monomers were synthesized by a click reaction between propargyl methacrylate and mono‐6‐azido‐β‐CD and then sulfonation or methylation was carried out. Finally, monolithic columns were prepared through a one‐step in situ copolymerization of the derivatized β‐CD monomer and ethylene glycol dimethacrylate. The sulfated β‐CD‐based monolith was successfully applied to the hydrophilic interaction liquid chromatography separation of nucleosides and small peptides, while the methylated β‐CD‐functionalized monolith was useful for the separation of nonpolar compounds and drug enantiomers in capillary reversed‐phase liquid chromatography. The structures of the monomers were characterized by Fourier transform infrared spectroscopy and mass spectrometry. The physicochemical properties and column performance of monoliths were evaluated by scanning electron microscopy and micro high performance liquid chromatography. This strategy has considerable prospects for the preparation of other derivatized CD‐functionalized methacrylate monoliths. |
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AbstractList | Derivatized [beta]-cyclodextrin ([beta]-CD) functionalized monolithic columns were prepared by a "one-step" strategy using click chemistry. First, the intended derivatized [beta]-CD monomers were synthesized by a click reaction between propargyl methacrylate and mono-6-azido-[beta]-CD and then sulfonation or methylation was carried out. Finally, monolithic columns were prepared through a one-step in situ copolymerization of the derivatized [beta]-CD monomer and ethylene glycol dimethacrylate. The sulfated [beta]-CD-based monolith was successfully applied to the hydrophilic interaction liquid chromatography separation of nucleosides and small peptides, while the methylated [beta]-CD-functionalized monolith was useful for the separation of nonpolar compounds and drug enantiomers in capillary reversed-phase liquid chromatography. The structures of the monomers were characterized by Fourier transform infrared spectroscopy and mass spectrometry. The physicochemical properties and column performance of monoliths were evaluated by scanning electron microscopy and micro high performance liquid chromatography. This strategy has considerable prospects for the preparation of other derivatized CD-functionalized methacrylate monoliths. Derivatized β‐cyclodextrin (β‐CD) functionalized monolithic columns were prepared by a “one‐step” strategy using click chemistry. First, the intended derivatized β‐CD monomers were synthesized by a click reaction between propargyl methacrylate and mono‐6‐azido‐β‐CD and then sulfonation or methylation was carried out. Finally, monolithic columns were prepared through a one‐step in situ copolymerization of the derivatized β‐CD monomer and ethylene glycol dimethacrylate. The sulfated β‐CD‐based monolith was successfully applied to the hydrophilic interaction liquid chromatography separation of nucleosides and small peptides, while the methylated β‐CD‐functionalized monolith was useful for the separation of nonpolar compounds and drug enantiomers in capillary reversed‐phase liquid chromatography. The structures of the monomers were characterized by Fourier transform infrared spectroscopy and mass spectrometry. The physicochemical properties and column performance of monoliths were evaluated by scanning electron microscopy and micro high performance liquid chromatography. This strategy has considerable prospects for the preparation of other derivatized CD‐functionalized methacrylate monoliths. Derivatized β-cyclodextrin (β-CD) functionalized monolithic columns were prepared by a "one-step" strategy using click chemistry. First, the intended derivatized β-CD monomers were synthesized by a click reaction between propargyl methacrylate and mono-6-azido-β-CD and then sulfonation or methylation was carried out. Finally, monolithic columns were prepared through a one-step in situ copolymerization of the derivatized β-CD monomer and ethylene glycol dimethacrylate. The sulfated β-CD-based monolith was successfully applied to the hydrophilic interaction liquid chromatography separation of nucleosides and small peptides, while the methylated β-CD-functionalized monolith was useful for the separation of nonpolar compounds and drug enantiomers in capillary reversed-phase liquid chromatography. The structures of the monomers were characterized by Fourier transform infrared spectroscopy and mass spectrometry. The physicochemical properties and column performance of monoliths were evaluated by scanning electron microscopy and micro high performance liquid chromatography. This strategy has considerable prospects for the preparation of other derivatized CD-functionalized methacrylate monoliths.Derivatized β-cyclodextrin (β-CD) functionalized monolithic columns were prepared by a "one-step" strategy using click chemistry. First, the intended derivatized β-CD monomers were synthesized by a click reaction between propargyl methacrylate and mono-6-azido-β-CD and then sulfonation or methylation was carried out. Finally, monolithic columns were prepared through a one-step in situ copolymerization of the derivatized β-CD monomer and ethylene glycol dimethacrylate. The sulfated β-CD-based monolith was successfully applied to the hydrophilic interaction liquid chromatography separation of nucleosides and small peptides, while the methylated β-CD-functionalized monolith was useful for the separation of nonpolar compounds and drug enantiomers in capillary reversed-phase liquid chromatography. The structures of the monomers were characterized by Fourier transform infrared spectroscopy and mass spectrometry. The physicochemical properties and column performance of monoliths were evaluated by scanning electron microscopy and micro high performance liquid chromatography. This strategy has considerable prospects for the preparation of other derivatized CD-functionalized methacrylate monoliths. Derivatized [beta]-cyclodextrin ([beta]-CD) functionalized monolithic columns were prepared by a "one-step" strategy using click chemistry. First, the intended derivatized [beta]-CD monomers were synthesized by a click reaction between propargyl methacrylate and mono-6-azido-[beta]-CD and then sulfonation or methylation was carried out. Finally, monolithic columns were prepared through a one-step in situ copolymerization of the derivatized [beta]-CD monomer and ethylene glycol dimethacrylate. The sulfated [beta]-CD-based monolith was successfully applied to the hydrophilic interaction liquid chromatography separation of nucleosides and small peptides, while the methylated [beta]-CD-functionalized monolith was useful for the separation of nonpolar compounds and drug enantiomers in capillary reversed-phase liquid chromatography. The structures of the monomers were characterized by Fourier transform infrared spectroscopy and mass spectrometry. The physicochemical properties and column performance of monoliths were evaluated by scanning electron microscopy and micro high performance liquid chromatography. This strategy has considerable prospects for the preparation of other derivatized CD-functionalized methacrylate monoliths. [PUBLICATION ABSTRACT] Derivatized β‐cyclodextrin (β‐CD) functionalized monolithic columns were prepared by a “one‐step” strategy using click chemistry. First, the intended derivatized β‐CD monomers were synthesized by a click reaction between propargyl methacrylate and mono‐6‐azido‐β‐CD and then sulfonation or methylation was carried out. Finally, monolithic columns were prepared through a one‐step in situ copolymerization of the derivatized β‐CD monomer and ethylene glycol dimethacrylate. The sulfated β‐CD‐based monolith was successfully applied to the hydrophilic interaction liquid chromatography separation of nucleosides and small peptides, while the methylated β‐CD‐functionalized monolith was useful for the separation of nonpolar compounds and drug enantiomers in capillary reversed‐phase liquid chromatography. The structures of the monomers were characterized by Fourier transform infrared spectroscopy and mass spectrometry. The physicochemical properties and column performance of monoliths were evaluated by scanning electron microscopy and micro high performance liquid chromatography. This strategy has considerable prospects for the preparation of other derivatized CD‐functionalized methacrylate monoliths. |
Author | Zhang, Qiaoxuan Zhao, Xianglong Jiang, Zhengjin Yao, Zhe Crommen, Jacques Ran, Danni Guo, Jialiang |
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Keywords | Capillary column Performance evaluation Purine derivatives Fourier transformation Separation Chromatographic retention HPLC chromatography Mass copolymerization Derivatization Retention time Characterization Crosslinked copolymer Functionalization Enantiomer Nucleoside Derivatized β-cyclodextrin Click chemistry Stationary phase Alkanophenone Hydrophilic Interaction Liquid chromatography Oligosaccharide Monolithic column Chiral stationary phase Acebutolol Ketone Monolithic columns Infrared spectrometry Reversed phase chromatography Cyclodextrin Ultraviolet detector Optical resolution Preparation Pyrimidine derivatives Methacrylate copolymer Inclusion compound Radical copolymerization Mass spectrometry Apolar compound Beta blocking agent |
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Snippet | Derivatized β‐cyclodextrin (β‐CD) functionalized monolithic columns were prepared by a “one‐step” strategy using click chemistry. First, the intended... Derivatized β-cyclodextrin (β-CD) functionalized monolithic columns were prepared by a "one-step" strategy using click chemistry. First, the intended... Derivatized [beta]-cyclodextrin ([beta]-CD) functionalized monolithic columns were prepared by a "one-step" strategy using click chemistry. First, the intended... Derivatized beta-cyclodextrin (beta-CD) functionalized monolithic columns were prepared by a "one-step" strategy using click chemistry. First, the intended... |
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SubjectTerms | Analysis Analytical chemistry beta-cyclodextrin beta-Cyclodextrins - chemical synthesis beta-Cyclodextrins - chemistry beta-Cyclodextrins/chemical synthesis/chemistry Biological and medical sciences Cadmium Chemical engineering Chemical synthesis Chemistry Chromatographic methods and physical methods associated with chromatography Chromatography Chromatography, High Pressure Liquid - instrumentation Click Chemistry Columns (structural) Derivatized beta-cyclodextrin Derivatized β-cyclodextrin drugs enantiomers Exact sciences and technology Fourier transform infrared spectroscopy Fourier transforms General pharmacology high performance liquid chromatography Human health sciences hydrophilic interactions Liquid chromatography Mass spectrometry Medical sciences Methacrylates - chemistry methylation Monolithic columns Monomers non-polar compounds Nucleosides Other chromatographic methods Peptides Pharmacie, pharmacologie & toxicologie Pharmacology. Drug treatments Pharmacy, pharmacology & toxicology physicochemical properties scanning electron microscopy Sciences de la santé humaine Separation Strategy |
Title | One‐step strategy for the synthesis of a derivatized cyclodextrin‐based monolithic column |
URI | https://api.istex.fr/ark:/67375/WNG-X005SFKP-3/fulltext.pdf https://onlinelibrary.wiley.com/doi/abs/10.1002%2Fjssc.201400312 https://www.ncbi.nlm.nih.gov/pubmed/24788588 https://www.proquest.com/docview/1545104831 https://www.proquest.com/docview/1547519119 https://www.proquest.com/docview/1559713313 https://www.proquest.com/docview/1663536800 http://orbi.ulg.ac.be/handle/2268/187180 |
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