Synthesis and characteristics of composite chiral stationary phases based on cellulose derivatives
Composite chiral stationary phases (CSPs) were prepared on the basis of cellulose derivatives coated or bonded onto silica. “Molecular exterior” type CSPs were prepared by mixing together two different cellulose tris‐derivatives before or after being coated or bonded onto silica, and the “molecular...
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Veröffentlicht in: | Journal of separation science 2003-01, Vol.26 (1-2), p.29-36 |
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creator | Chen, Xiaoming Zou, Hanfa Ni, Jianyi Feng, Shun |
description | Composite chiral stationary phases (CSPs) were prepared on the basis of cellulose derivatives coated or bonded onto silica. “Molecular exterior” type CSPs were prepared by mixing together two different cellulose tris‐derivatives before or after being coated or bonded onto silica, and the “molecular interior” type was obtained by synthesizing non‐regioselectively heterosubstituted cellulose derivatives coated or bonded onto silica. For the sake of comparison, the individual phases were also prepared with corresponding cellulose derivatives by coating or bonding approaches, respectively. All of the prepared CSPs were characterized and their chiral recognition properties were evaluated by HPLC with several test racemates. The experimental results demonstrated that the “molecular exterior” CSPs generally exhibit chiral recognition capacities intermediate between those of the two individual phases. However, in the separation of some racemates higher enantioselectivity may be achieved on the “molecular interior” phases than on individual phases, thus broadening the application range of a single cellulose‐based CSP. |
doi_str_mv | 10.1002/jssc.200390010 |
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For the sake of comparison, the individual phases were also prepared with corresponding cellulose derivatives by coating or bonding approaches, respectively. All of the prepared CSPs were characterized and their chiral recognition properties were evaluated by HPLC with several test racemates. The experimental results demonstrated that the “molecular exterior” CSPs generally exhibit chiral recognition capacities intermediate between those of the two individual phases. However, in the separation of some racemates higher enantioselectivity may be achieved on the “molecular interior” phases than on individual phases, thus broadening the application range of a single cellulose‐based CSP.</description><identifier>ISSN: 1615-9306</identifier><identifier>EISSN: 1615-9314</identifier><identifier>DOI: 10.1002/jssc.200390010</identifier><language>eng</language><publisher>Weinheim: WILEY-VCH Verlag</publisher><subject>Analysis ; Analytical chemistry ; Biological and medical sciences ; Cellulose derivatives ; Chemistry ; Chromatographic methods and physical methods associated with chromatography ; Composite chiral stationary phase ; Enantioseparation ; Exact sciences and technology ; General pharmacology ; Liquid chromatography ; Medical sciences ; Other chromatographic methods ; Pharmacology. Drug treatments</subject><ispartof>Journal of separation science, 2003-01, Vol.26 (1-2), p.29-36</ispartof><rights>Copyright © 2003 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim</rights><rights>2003 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4210-fa96d1b6ca0e8fe81191cc32e6f4c3bf856c3d551f02691817d5b64501c05a083</citedby><cites>FETCH-LOGICAL-c4210-fa96d1b6ca0e8fe81191cc32e6f4c3bf856c3d551f02691817d5b64501c05a083</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fjssc.200390010$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fjssc.200390010$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,777,781,1412,4010,27904,27905,27906,45555,45556</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=14532737$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>Chen, Xiaoming</creatorcontrib><creatorcontrib>Zou, Hanfa</creatorcontrib><creatorcontrib>Ni, Jianyi</creatorcontrib><creatorcontrib>Feng, Shun</creatorcontrib><title>Synthesis and characteristics of composite chiral stationary phases based on cellulose derivatives</title><title>Journal of separation science</title><addtitle>J. Sep. Science</addtitle><description>Composite chiral stationary phases (CSPs) were prepared on the basis of cellulose derivatives coated or bonded onto silica. “Molecular exterior” type CSPs were prepared by mixing together two different cellulose tris‐derivatives before or after being coated or bonded onto silica, and the “molecular interior” type was obtained by synthesizing non‐regioselectively heterosubstituted cellulose derivatives coated or bonded onto silica. For the sake of comparison, the individual phases were also prepared with corresponding cellulose derivatives by coating or bonding approaches, respectively. All of the prepared CSPs were characterized and their chiral recognition properties were evaluated by HPLC with several test racemates. The experimental results demonstrated that the “molecular exterior” CSPs generally exhibit chiral recognition capacities intermediate between those of the two individual phases. However, in the separation of some racemates higher enantioselectivity may be achieved on the “molecular interior” phases than on individual phases, thus broadening the application range of a single cellulose‐based CSP.</description><subject>Analysis</subject><subject>Analytical chemistry</subject><subject>Biological and medical sciences</subject><subject>Cellulose derivatives</subject><subject>Chemistry</subject><subject>Chromatographic methods and physical methods associated with chromatography</subject><subject>Composite chiral stationary phase</subject><subject>Enantioseparation</subject><subject>Exact sciences and technology</subject><subject>General pharmacology</subject><subject>Liquid chromatography</subject><subject>Medical sciences</subject><subject>Other chromatographic methods</subject><subject>Pharmacology. Drug treatments</subject><issn>1615-9306</issn><issn>1615-9314</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2003</creationdate><recordtype>article</recordtype><recordid>eNqFkM1PwzAMxSsEEmNw5ZwLxw6nabL2iCY-NcakjY9blKaJltG1U1wG--_JVDS4cbEt-f2erRdF5xQGFCC5XCLqQQLAcgAKB1GPCsrjnNH0cD-DOI5OEJdBMcxy6EXFbFu3C4MOiapLohfKK90a77B1GkljiW5W6wZda8LSeVURbFXrmlr5LVkvFBokRaglaWqiTVV9VA0aUgaLTdBtDJ5GR1ZVaM5-ej96vrmej-7i8dPt_ehqHOs0oRBblYuSFkIrMJk1GaU51ZolRthUs8JmXGhWck4tJCKnGR2WvBApB6qBK8hYPxp0vto3iN5YufZuFd6UFOQuIblLSO4TCsBFB6wValVZr2rt8JdKOUuGbBh0eaf7dJXZ_uMqH2az0d8bcceGQM3XnlX-XYrgzeXr5FZO3yYv8-ljKjn7BvjHiPg</recordid><startdate>20030101</startdate><enddate>20030101</enddate><creator>Chen, Xiaoming</creator><creator>Zou, Hanfa</creator><creator>Ni, Jianyi</creator><creator>Feng, Shun</creator><general>WILEY-VCH Verlag</general><general>WILEY‐VCH Verlag</general><general>Wiley</general><scope>BSCLL</scope><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20030101</creationdate><title>Synthesis and characteristics of composite chiral stationary phases based on cellulose derivatives</title><author>Chen, Xiaoming ; Zou, Hanfa ; Ni, Jianyi ; Feng, Shun</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4210-fa96d1b6ca0e8fe81191cc32e6f4c3bf856c3d551f02691817d5b64501c05a083</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2003</creationdate><topic>Analysis</topic><topic>Analytical chemistry</topic><topic>Biological and medical sciences</topic><topic>Cellulose derivatives</topic><topic>Chemistry</topic><topic>Chromatographic methods and physical methods associated with chromatography</topic><topic>Composite chiral stationary phase</topic><topic>Enantioseparation</topic><topic>Exact sciences and technology</topic><topic>General pharmacology</topic><topic>Liquid chromatography</topic><topic>Medical sciences</topic><topic>Other chromatographic methods</topic><topic>Pharmacology. Drug treatments</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Chen, Xiaoming</creatorcontrib><creatorcontrib>Zou, Hanfa</creatorcontrib><creatorcontrib>Ni, Jianyi</creatorcontrib><creatorcontrib>Feng, Shun</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>CrossRef</collection><jtitle>Journal of separation science</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chen, Xiaoming</au><au>Zou, Hanfa</au><au>Ni, Jianyi</au><au>Feng, Shun</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Synthesis and characteristics of composite chiral stationary phases based on cellulose derivatives</atitle><jtitle>Journal of separation science</jtitle><addtitle>J. Sep. Science</addtitle><date>2003-01-01</date><risdate>2003</risdate><volume>26</volume><issue>1-2</issue><spage>29</spage><epage>36</epage><pages>29-36</pages><issn>1615-9306</issn><eissn>1615-9314</eissn><abstract>Composite chiral stationary phases (CSPs) were prepared on the basis of cellulose derivatives coated or bonded onto silica. “Molecular exterior” type CSPs were prepared by mixing together two different cellulose tris‐derivatives before or after being coated or bonded onto silica, and the “molecular interior” type was obtained by synthesizing non‐regioselectively heterosubstituted cellulose derivatives coated or bonded onto silica. For the sake of comparison, the individual phases were also prepared with corresponding cellulose derivatives by coating or bonding approaches, respectively. All of the prepared CSPs were characterized and their chiral recognition properties were evaluated by HPLC with several test racemates. The experimental results demonstrated that the “molecular exterior” CSPs generally exhibit chiral recognition capacities intermediate between those of the two individual phases. However, in the separation of some racemates higher enantioselectivity may be achieved on the “molecular interior” phases than on individual phases, thus broadening the application range of a single cellulose‐based CSP.</abstract><cop>Weinheim</cop><pub>WILEY-VCH Verlag</pub><doi>10.1002/jssc.200390010</doi><tpages>8</tpages></addata></record> |
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subjects | Analysis Analytical chemistry Biological and medical sciences Cellulose derivatives Chemistry Chromatographic methods and physical methods associated with chromatography Composite chiral stationary phase Enantioseparation Exact sciences and technology General pharmacology Liquid chromatography Medical sciences Other chromatographic methods Pharmacology. Drug treatments |
title | Synthesis and characteristics of composite chiral stationary phases based on cellulose derivatives |
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