Soluble and Processable Phosphonate Sensing Star Molecularly Imprinted Polymers
Soluble molecularly imprinted polymers (MIPs) were prepared by reversible addition fragmentation chain transfer (RAFT) polymerization followed by ring-closing metathesis (RCM). The polymerization was done in the presence of a template to generate a processable star MIP. The core of the star polymer...
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Veröffentlicht in: | Macromolecules 2007-03, Vol.40 (5), p.1395-1400 |
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creator | Southard, Glen E. Van Houten, Kelly A. Murray, George M. |
description | Soluble molecularly imprinted polymers (MIPs) were prepared by reversible addition fragmentation chain transfer (RAFT) polymerization followed by ring-closing metathesis (RCM). The polymerization was done in the presence of a template to generate a processable star MIP. The core of the star polymer was a dithiobenzoate-substituted tris(β-diketonate)europium(III) complex. The tris(β-diketonate)europium(III) complex served as a polymerization substrate for the three-armed RAFT-mediated star polymer and as a luminescent binding site for dicrotophos, an organophosphonate pesticide. The star arms were AB block copolymers. Block A was either 1-but-3-enyl-4-vinylbenzene or a mixture of 1-but-3-enyl-4-vinylbenzene and styrene. Block B was styrene or methyl methacrylate. The but-3-enyls of block A were reacted by RCM with a second generation Grubbs catalyst to give an intramolecularly cross-linked core. The intramolecularly cross-linked MIP was soluble in common organic solvents. The 30% cross-linked soluble and processable star MIP was applied to the determination of dicrotophos with sub-ppb level detection limits. |
doi_str_mv | 10.1021/ma062443e |
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The polymerization was done in the presence of a template to generate a processable star MIP. The core of the star polymer was a dithiobenzoate-substituted tris(β-diketonate)europium(III) complex. The tris(β-diketonate)europium(III) complex served as a polymerization substrate for the three-armed RAFT-mediated star polymer and as a luminescent binding site for dicrotophos, an organophosphonate pesticide. The star arms were AB block copolymers. Block A was either 1-but-3-enyl-4-vinylbenzene or a mixture of 1-but-3-enyl-4-vinylbenzene and styrene. Block B was styrene or methyl methacrylate. The but-3-enyls of block A were reacted by RCM with a second generation Grubbs catalyst to give an intramolecularly cross-linked core. The intramolecularly cross-linked MIP was soluble in common organic solvents. The 30% cross-linked soluble and processable star MIP was applied to the determination of dicrotophos with sub-ppb level detection limits.</description><identifier>ISSN: 0024-9297</identifier><identifier>EISSN: 1520-5835</identifier><identifier>DOI: 10.1021/ma062443e</identifier><identifier>CODEN: MAMOBX</identifier><language>eng</language><publisher>Washington, DC: American Chemical Society</publisher><subject>Applied sciences ; Exact sciences and technology ; Organic polymers ; Physicochemistry of polymers ; Polymers with particular properties ; Preparation, kinetics, thermodynamics, mechanism and catalysts</subject><ispartof>Macromolecules, 2007-03, Vol.40 (5), p.1395-1400</ispartof><rights>Copyright © 2007 American Chemical Society</rights><rights>2007 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a289t-358f52b34c623e232d260c6a1435dccc6352b3302a35ee64134c59b54b6c542c3</citedby><cites>FETCH-LOGICAL-a289t-358f52b34c623e232d260c6a1435dccc6352b3302a35ee64134c59b54b6c542c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://pubs.acs.org/doi/pdf/10.1021/ma062443e$$EPDF$$P50$$Gacs$$H</linktopdf><linktohtml>$$Uhttps://pubs.acs.org/doi/10.1021/ma062443e$$EHTML$$P50$$Gacs$$H</linktohtml><link.rule.ids>314,780,784,2765,27076,27924,27925,56738,56788</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=18625516$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>Southard, Glen E.</creatorcontrib><creatorcontrib>Van Houten, Kelly A.</creatorcontrib><creatorcontrib>Murray, George M.</creatorcontrib><title>Soluble and Processable Phosphonate Sensing Star Molecularly Imprinted Polymers</title><title>Macromolecules</title><addtitle>Macromolecules</addtitle><description>Soluble molecularly imprinted polymers (MIPs) were prepared by reversible addition fragmentation chain transfer (RAFT) polymerization followed by ring-closing metathesis (RCM). The polymerization was done in the presence of a template to generate a processable star MIP. The core of the star polymer was a dithiobenzoate-substituted tris(β-diketonate)europium(III) complex. The tris(β-diketonate)europium(III) complex served as a polymerization substrate for the three-armed RAFT-mediated star polymer and as a luminescent binding site for dicrotophos, an organophosphonate pesticide. The star arms were AB block copolymers. Block A was either 1-but-3-enyl-4-vinylbenzene or a mixture of 1-but-3-enyl-4-vinylbenzene and styrene. Block B was styrene or methyl methacrylate. The but-3-enyls of block A were reacted by RCM with a second generation Grubbs catalyst to give an intramolecularly cross-linked core. The intramolecularly cross-linked MIP was soluble in common organic solvents. The 30% cross-linked soluble and processable star MIP was applied to the determination of dicrotophos with sub-ppb level detection limits.</description><subject>Applied sciences</subject><subject>Exact sciences and technology</subject><subject>Organic polymers</subject><subject>Physicochemistry of polymers</subject><subject>Polymers with particular properties</subject><subject>Preparation, kinetics, thermodynamics, mechanism and catalysts</subject><issn>0024-9297</issn><issn>1520-5835</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><recordid>eNptkD9PwzAQxS0EEqUw8A2yMDAE7LPPJCOq-FOpqJUKc3RxHdrKsSs7GfrtSVVEF6bT6X7v6d5j7FbwB8FBPLbENSgl7RkbCQSeYyHxnI04B5WXUD5dsquUtpwLgUqO2HwZXF87m5FfZYsYjE2JDvtiHdJuHTx1Nltanzb-O1t2FLOP4KzpHUW3z6btLm58ZwdpcPvWxnTNLhpyyd78zjH7en35nLzns_nbdPI8ywmKssslFg1CLZXRIC1IWIHmRpNQElfGGC0PV8mBJFqrlRhILGtUtTaowMgxuz_6mhhSiraphk9aivtK8OrQRPXXxMDeHdkdJUOuieTNJp0EhQZEoU8cmVRtQx_9kOAfvx9OnGlq</recordid><startdate>20070306</startdate><enddate>20070306</enddate><creator>Southard, Glen E.</creator><creator>Van Houten, Kelly A.</creator><creator>Murray, George M.</creator><general>American Chemical Society</general><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20070306</creationdate><title>Soluble and Processable Phosphonate Sensing Star Molecularly Imprinted Polymers</title><author>Southard, Glen E. ; Van Houten, Kelly A. ; Murray, George M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a289t-358f52b34c623e232d260c6a1435dccc6352b3302a35ee64134c59b54b6c542c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>Applied sciences</topic><topic>Exact sciences and technology</topic><topic>Organic polymers</topic><topic>Physicochemistry of polymers</topic><topic>Polymers with particular properties</topic><topic>Preparation, kinetics, thermodynamics, mechanism and catalysts</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Southard, Glen E.</creatorcontrib><creatorcontrib>Van Houten, Kelly A.</creatorcontrib><creatorcontrib>Murray, George M.</creatorcontrib><collection>Pascal-Francis</collection><collection>CrossRef</collection><jtitle>Macromolecules</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Southard, Glen E.</au><au>Van Houten, Kelly A.</au><au>Murray, George M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Soluble and Processable Phosphonate Sensing Star Molecularly Imprinted Polymers</atitle><jtitle>Macromolecules</jtitle><addtitle>Macromolecules</addtitle><date>2007-03-06</date><risdate>2007</risdate><volume>40</volume><issue>5</issue><spage>1395</spage><epage>1400</epage><pages>1395-1400</pages><issn>0024-9297</issn><eissn>1520-5835</eissn><coden>MAMOBX</coden><abstract>Soluble molecularly imprinted polymers (MIPs) were prepared by reversible addition fragmentation chain transfer (RAFT) polymerization followed by ring-closing metathesis (RCM). The polymerization was done in the presence of a template to generate a processable star MIP. The core of the star polymer was a dithiobenzoate-substituted tris(β-diketonate)europium(III) complex. The tris(β-diketonate)europium(III) complex served as a polymerization substrate for the three-armed RAFT-mediated star polymer and as a luminescent binding site for dicrotophos, an organophosphonate pesticide. The star arms were AB block copolymers. Block A was either 1-but-3-enyl-4-vinylbenzene or a mixture of 1-but-3-enyl-4-vinylbenzene and styrene. Block B was styrene or methyl methacrylate. The but-3-enyls of block A were reacted by RCM with a second generation Grubbs catalyst to give an intramolecularly cross-linked core. The intramolecularly cross-linked MIP was soluble in common organic solvents. The 30% cross-linked soluble and processable star MIP was applied to the determination of dicrotophos with sub-ppb level detection limits.</abstract><cop>Washington, DC</cop><pub>American Chemical Society</pub><doi>10.1021/ma062443e</doi><tpages>6</tpages></addata></record> |
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subjects | Applied sciences Exact sciences and technology Organic polymers Physicochemistry of polymers Polymers with particular properties Preparation, kinetics, thermodynamics, mechanism and catalysts |
title | Soluble and Processable Phosphonate Sensing Star Molecularly Imprinted Polymers |
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