Synthesis and application of novel bonded cationic β-cyclodextrin derivatives as chiral stationary phases for supercritical fluid chromatography

A novel cationic β-cyclodextrin derivative named mono-6A-(3-vinylimidazolium)-6A-deoxyperphenylcarbamoylated-β-cyclodextrin chloride was synthesized by selective tosylation and vinylimidazole substitution followed by perfunctionalisation with phenylcarbamate groups. The fully derivatized β-cyclodext...

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Main Author: Liu, Maolong.
Other Authors: Ng Siu Choon
Format: Final Year Project
Language:English
Published: 2009
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Online Access:http://hdl.handle.net/10356/16714
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Institution: Nanyang Technological University
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spelling sg-ntu-dr.10356-167142023-03-03T15:40:11Z Synthesis and application of novel bonded cationic β-cyclodextrin derivatives as chiral stationary phases for supercritical fluid chromatography Liu, Maolong. Ng Siu Choon School of Chemical and Biomedical Engineering DRNTU::Science::Chemistry::Analytical chemistry::Chromatography A novel cationic β-cyclodextrin derivative named mono-6A-(3-vinylimidazolium)-6A-deoxyperphenylcarbamoylated-β-cyclodextrin chloride was synthesized by selective tosylation and vinylimidazole substitution followed by perfunctionalisation with phenylcarbamate groups. The fully derivatized β-cyclodextrin was then immobilized onto a vinylized silica gel to provide new chiral stationary phases (CSPs). The immobilization of the derivative was performed through a radical co-polymerization reaction with AIBN as the initiator in the help of different small molecular monomers. Two monomers were used to help co-polymerization, namely 2,3-dimethyl-1,3-butadiene (DMBD) and methylmethacrylate (MMA). Their effects on immobilization and enantioselective capabilities of CSPs were investigated. The performance of CSPs prepared was evaluated on supercritical fluid chromatography (SFC) using a wide range of racemic drugs as test analysts such as β-blockers, flavanone compounds, profens, dansyl-amino acids, etc which are of high medical values. Good separations were achieved for flavanone compounds, dansyl-amino acids and some of the non-protolytic drugs. The enantiodiscriminatory properties of the CSPs were found to be affected mainly by the phenylcarbamate groups of β-cyclodextrin derivative and also the cationic imidazole spacer arm at the primary rim. The selection of modifier in mobile phase was found to be racemate type-dependent, and addition of small amount acidic additive into modifier can improve the separation efficiency and reduce peak broadening of acidic samples without compromising the selectivity. Generally, CSP immobilized using DMBD has a better performance than that of MMA. Bachelor of Engineering (Chemical and Biomolecular Engineering) 2009-05-28T02:40:50Z 2009-05-28T02:40:50Z 2009 2009 Final Year Project (FYP) http://hdl.handle.net/10356/16714 en Nanyang Technological University 70 p. application/pdf
institution Nanyang Technological University
building NTU Library
continent Asia
country Singapore
Singapore
content_provider NTU Library
collection DR-NTU
language English
topic DRNTU::Science::Chemistry::Analytical chemistry::Chromatography
spellingShingle DRNTU::Science::Chemistry::Analytical chemistry::Chromatography
Liu, Maolong.
Synthesis and application of novel bonded cationic β-cyclodextrin derivatives as chiral stationary phases for supercritical fluid chromatography
description A novel cationic β-cyclodextrin derivative named mono-6A-(3-vinylimidazolium)-6A-deoxyperphenylcarbamoylated-β-cyclodextrin chloride was synthesized by selective tosylation and vinylimidazole substitution followed by perfunctionalisation with phenylcarbamate groups. The fully derivatized β-cyclodextrin was then immobilized onto a vinylized silica gel to provide new chiral stationary phases (CSPs). The immobilization of the derivative was performed through a radical co-polymerization reaction with AIBN as the initiator in the help of different small molecular monomers. Two monomers were used to help co-polymerization, namely 2,3-dimethyl-1,3-butadiene (DMBD) and methylmethacrylate (MMA). Their effects on immobilization and enantioselective capabilities of CSPs were investigated. The performance of CSPs prepared was evaluated on supercritical fluid chromatography (SFC) using a wide range of racemic drugs as test analysts such as β-blockers, flavanone compounds, profens, dansyl-amino acids, etc which are of high medical values. Good separations were achieved for flavanone compounds, dansyl-amino acids and some of the non-protolytic drugs. The enantiodiscriminatory properties of the CSPs were found to be affected mainly by the phenylcarbamate groups of β-cyclodextrin derivative and also the cationic imidazole spacer arm at the primary rim. The selection of modifier in mobile phase was found to be racemate type-dependent, and addition of small amount acidic additive into modifier can improve the separation efficiency and reduce peak broadening of acidic samples without compromising the selectivity. Generally, CSP immobilized using DMBD has a better performance than that of MMA.
author2 Ng Siu Choon
author_facet Ng Siu Choon
Liu, Maolong.
format Final Year Project
author Liu, Maolong.
author_sort Liu, Maolong.
title Synthesis and application of novel bonded cationic β-cyclodextrin derivatives as chiral stationary phases for supercritical fluid chromatography
title_short Synthesis and application of novel bonded cationic β-cyclodextrin derivatives as chiral stationary phases for supercritical fluid chromatography
title_full Synthesis and application of novel bonded cationic β-cyclodextrin derivatives as chiral stationary phases for supercritical fluid chromatography
title_fullStr Synthesis and application of novel bonded cationic β-cyclodextrin derivatives as chiral stationary phases for supercritical fluid chromatography
title_full_unstemmed Synthesis and application of novel bonded cationic β-cyclodextrin derivatives as chiral stationary phases for supercritical fluid chromatography
title_sort synthesis and application of novel bonded cationic β-cyclodextrin derivatives as chiral stationary phases for supercritical fluid chromatography
publishDate 2009
url http://hdl.handle.net/10356/16714
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