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 inJournal of separation science Vol. 37; no. 14; pp. 1720 - 1727
Main Authors Guo, Jialiang, Zhang, Qiaoxuan, Yao, Zhe, Zhao, Xianglong, Ran, Danni, Crommen, Jacques, Jiang, Zhengjin
Format Journal Article Web Resource
LanguageEnglish
Published Weinheim Wiley-VCH 01.07.2014
Blackwell Publishing Ltd
Wiley
Wiley Subscription Services, Inc
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ISSN1615-9306
1615-9314
1615-9314
DOI10.1002/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.
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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Issue 14
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
Language English
License http://onlinelibrary.wiley.com/termsAndConditions#vor
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2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
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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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StartPage 1720
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
Volume 37
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