One-step synthesis of an organic-inorganic hybrid boronate affinity monolithic column with synergistic co-monomers
An organic-inorganic hybrid and synergistic boronate affinity (BA) monolithic column was synthesized by a novel "one-step" approach. We report on the synthesis of a unique organic-inorganic hybrid affinity monolith by using TEOS, the organic silane, N-(β-aminoethyl)-γ-aminopropyltriethoxys...
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Veröffentlicht in: | Analyst (London) 2013-09, Vol.138 (17), p.4752-4755 |
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creator | Yang, Qin Huang, Dihui Jin, Shanxia Zhou, Hailong Zhou, Ping |
description | An organic-inorganic hybrid and synergistic boronate affinity (BA) monolithic column was synthesized by a novel "one-step" approach. We report on the synthesis of a unique organic-inorganic hybrid affinity monolith by using TEOS, the organic silane, N-(β-aminoethyl)-γ-aminopropyltriethoxysilane (AEAPTES) and γ-MAPS as the co-precursors, 4-vinylphenylboronic acid as the functionalized monomer, and azobisisobutyronitrile (AIBN) as the initiator. Due to the presence of amino groups in the AEAPTES molecule, the prepared monolith exhibits several attractive properties. The monolith will be more hydrophilic and can bind with cis-diol compounds at neutral pH by a mechanism of intermolecular B-N coordination. The resulting hybrid boronate affinity monoliths have potential applications in specific recognition and enrichment of cis-diol biomolecules under neutral conditions. |
doi_str_mv | 10.1039/c3an00847a |
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We report on the synthesis of a unique organic-inorganic hybrid affinity monolith by using TEOS, the organic silane, N-(β-aminoethyl)-γ-aminopropyltriethoxysilane (AEAPTES) and γ-MAPS as the co-precursors, 4-vinylphenylboronic acid as the functionalized monomer, and azobisisobutyronitrile (AIBN) as the initiator. Due to the presence of amino groups in the AEAPTES molecule, the prepared monolith exhibits several attractive properties. The monolith will be more hydrophilic and can bind with cis-diol compounds at neutral pH by a mechanism of intermolecular B-N coordination. The resulting hybrid boronate affinity monoliths have potential applications in specific recognition and enrichment of cis-diol biomolecules under neutral conditions.</description><identifier>ISSN: 0003-2654</identifier><identifier>EISSN: 1364-5528</identifier><identifier>DOI: 10.1039/c3an00847a</identifier><identifier>PMID: 23869381</identifier><language>eng</language><publisher>England</publisher><subject>Affinity ; Azobisisobutyronitrile ; Biomolecules ; Boronic Acids - chemical synthesis ; Boronic Acids - chemistry ; Chemistry Techniques, Synthetic ; Chromatography, Liquid - methods ; Monomers ; Recognition ; Silanes ; Silanes - chemistry ; Synthesis</subject><ispartof>Analyst (London), 2013-09, Vol.138 (17), p.4752-4755</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c320t-7d871d3be864e734e7b5a0a979a890ac52f232d4105cf5077107b4498ed50f773</citedby><cites>FETCH-LOGICAL-c320t-7d871d3be864e734e7b5a0a979a890ac52f232d4105cf5077107b4498ed50f773</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,2830,27923,27924</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23869381$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Yang, Qin</creatorcontrib><creatorcontrib>Huang, Dihui</creatorcontrib><creatorcontrib>Jin, Shanxia</creatorcontrib><creatorcontrib>Zhou, Hailong</creatorcontrib><creatorcontrib>Zhou, Ping</creatorcontrib><title>One-step synthesis of an organic-inorganic hybrid boronate affinity monolithic column with synergistic co-monomers</title><title>Analyst (London)</title><addtitle>Analyst</addtitle><description>An organic-inorganic hybrid and synergistic boronate affinity (BA) monolithic column was synthesized by a novel "one-step" approach. 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The resulting hybrid boronate affinity monoliths have potential applications in specific recognition and enrichment of cis-diol biomolecules under neutral conditions.</description><subject>Affinity</subject><subject>Azobisisobutyronitrile</subject><subject>Biomolecules</subject><subject>Boronic Acids - chemical synthesis</subject><subject>Boronic Acids - chemistry</subject><subject>Chemistry Techniques, Synthetic</subject><subject>Chromatography, Liquid - methods</subject><subject>Monomers</subject><subject>Recognition</subject><subject>Silanes</subject><subject>Silanes - chemistry</subject><subject>Synthesis</subject><issn>0003-2654</issn><issn>1364-5528</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkU1PwzAMhiMEYmNw4QegHBFSwPlq2iOa-JIm7QLnKm3TLahNRpIJ9d_TsQFXDpb9Wo9fyTZClxRuKfDirubaAeRC6SM0pTwTREqWH6MpAHDCMikm6CzG91FSkHCKJoznWcFzOkVh6QyJyWxwHFxam2gj9i3WDvuw0s7WxLpDhddDFWyDKx-808lg3bbW2TTg3jvf2bQemdp3297hz1HtHE1Y2Zi--2RH9SbEc3TS6i6ai0OeobfHh9f5M1ksn17m9wtScwaJqCZXtOGVyTNhFB-jkhp0oQqdF6BryVrGWSPGlepWglIUVCVEkZtGQqsUn6Hrve8m-I-tiansbaxN12ln_DaWNFM0G6ezf6CCZiC4KtiI3uzROvgYg2nLTbC9DkNJody9o_x7xwhfHXy3VW-aX_Tn_vwLQ1qG1g</recordid><startdate>20130907</startdate><enddate>20130907</enddate><creator>Yang, Qin</creator><creator>Huang, Dihui</creator><creator>Jin, Shanxia</creator><creator>Zhou, Hailong</creator><creator>Zhou, Ping</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>7SR</scope><scope>7U5</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope><scope>L7M</scope></search><sort><creationdate>20130907</creationdate><title>One-step synthesis of an organic-inorganic hybrid boronate affinity monolithic column with synergistic co-monomers</title><author>Yang, Qin ; Huang, Dihui ; Jin, Shanxia ; Zhou, Hailong ; Zhou, Ping</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c320t-7d871d3be864e734e7b5a0a979a890ac52f232d4105cf5077107b4498ed50f773</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Affinity</topic><topic>Azobisisobutyronitrile</topic><topic>Biomolecules</topic><topic>Boronic Acids - chemical synthesis</topic><topic>Boronic Acids - chemistry</topic><topic>Chemistry Techniques, Synthetic</topic><topic>Chromatography, Liquid - methods</topic><topic>Monomers</topic><topic>Recognition</topic><topic>Silanes</topic><topic>Silanes - chemistry</topic><topic>Synthesis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Yang, Qin</creatorcontrib><creatorcontrib>Huang, Dihui</creatorcontrib><creatorcontrib>Jin, Shanxia</creatorcontrib><creatorcontrib>Zhou, Hailong</creatorcontrib><creatorcontrib>Zhou, Ping</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Engineered Materials Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><jtitle>Analyst (London)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yang, Qin</au><au>Huang, Dihui</au><au>Jin, Shanxia</au><au>Zhou, Hailong</au><au>Zhou, Ping</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>One-step synthesis of an organic-inorganic hybrid boronate affinity monolithic column with synergistic co-monomers</atitle><jtitle>Analyst (London)</jtitle><addtitle>Analyst</addtitle><date>2013-09-07</date><risdate>2013</risdate><volume>138</volume><issue>17</issue><spage>4752</spage><epage>4755</epage><pages>4752-4755</pages><issn>0003-2654</issn><eissn>1364-5528</eissn><abstract>An organic-inorganic hybrid and synergistic boronate affinity (BA) monolithic column was synthesized by a novel "one-step" approach. We report on the synthesis of a unique organic-inorganic hybrid affinity monolith by using TEOS, the organic silane, N-(β-aminoethyl)-γ-aminopropyltriethoxysilane (AEAPTES) and γ-MAPS as the co-precursors, 4-vinylphenylboronic acid as the functionalized monomer, and azobisisobutyronitrile (AIBN) as the initiator. Due to the presence of amino groups in the AEAPTES molecule, the prepared monolith exhibits several attractive properties. The monolith will be more hydrophilic and can bind with cis-diol compounds at neutral pH by a mechanism of intermolecular B-N coordination. The resulting hybrid boronate affinity monoliths have potential applications in specific recognition and enrichment of cis-diol biomolecules under neutral conditions.</abstract><cop>England</cop><pmid>23869381</pmid><doi>10.1039/c3an00847a</doi><tpages>4</tpages></addata></record> |
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source | MEDLINE; Royal Society of Chemistry Journals Archive (1841-2007); Royal Society Of Chemistry Journals 2008-; Alma/SFX Local Collection |
subjects | Affinity Azobisisobutyronitrile Biomolecules Boronic Acids - chemical synthesis Boronic Acids - chemistry Chemistry Techniques, Synthetic Chromatography, Liquid - methods Monomers Recognition Silanes Silanes - chemistry Synthesis |
title | One-step synthesis of an organic-inorganic hybrid boronate affinity monolithic column with synergistic co-monomers |
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