Poly(vinylphosphonate)s with Widely Tunable LCST: A Promising Alternative to Conventional Thermoresponsive Polymers
Novel statistic copolymers of dialkyl vinylphosphonates have been synthesized via rare earth metal-mediated group transfer polymerization using easily accessible tris(cyclopentadienyl)ytterbium. The copolymerization parameters have been determined by activity measurements showing the formation of al...
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Veröffentlicht in: | Macromolecules 2012-12, Vol.45 (24), p.9751-9758 |
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description | Novel statistic copolymers of dialkyl vinylphosphonates have been synthesized via rare earth metal-mediated group transfer polymerization using easily accessible tris(cyclopentadienyl)ytterbium. The copolymerization parameters have been determined by activity measurements showing the formation of almost perfectly random copolymers (r 1, r 2 ∼ 1). Thus, the polymerization rate of vinylphosphonate GTP is mainly limited by the steric demand of growing polymer chain end. The obtained copolymers of diethyl vinylphosphonate and dimethyl or di-n-propyl vinylphosphonate show thermoresponsive properties, i.e., exhibit a tunable lower critical solution temperature following a coil–globule transition mechanism, with cloud points between 5 and 92 °C. Hereby, the LCST can be precisely adjusted by varying the comonomer composition and correlates linearly with the content of hydrophilic/hydrophobic comonomer. These thermoresponsive poly(vinylphosphonate)s, exhibiting a sharp and reversible phase transition, and minor environmental effects such as concentration and additives on their cloud point, are promising candidates in biomedical applications. |
doi_str_mv | 10.1021/ma3019014 |
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The copolymerization parameters have been determined by activity measurements showing the formation of almost perfectly random copolymers (r 1, r 2 ∼ 1). Thus, the polymerization rate of vinylphosphonate GTP is mainly limited by the steric demand of growing polymer chain end. The obtained copolymers of diethyl vinylphosphonate and dimethyl or di-n-propyl vinylphosphonate show thermoresponsive properties, i.e., exhibit a tunable lower critical solution temperature following a coil–globule transition mechanism, with cloud points between 5 and 92 °C. Hereby, the LCST can be precisely adjusted by varying the comonomer composition and correlates linearly with the content of hydrophilic/hydrophobic comonomer. These thermoresponsive poly(vinylphosphonate)s, exhibiting a sharp and reversible phase transition, and minor environmental effects such as concentration and additives on their cloud point, are promising candidates in biomedical applications.</description><identifier>ISSN: 0024-9297</identifier><identifier>EISSN: 1520-5835</identifier><identifier>DOI: 10.1021/ma3019014</identifier><identifier>CODEN: MAMOBX</identifier><language>eng</language><publisher>Washington, DC: American Chemical Society</publisher><subject>Applied sciences ; Copolymerization ; Exact sciences and technology ; Organic polymers ; Physicochemistry of polymers ; Preparation, kinetics, thermodynamics, mechanism and catalysts</subject><ispartof>Macromolecules, 2012-12, Vol.45 (24), p.9751-9758</ispartof><rights>Copyright © 2012 American Chemical Society</rights><rights>2014 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a326t-f38ed6fee771ae763fc47b6b672aee3793736f22ae0dd406b4397b352967e3213</citedby><cites>FETCH-LOGICAL-a326t-f38ed6fee771ae763fc47b6b672aee3793736f22ae0dd406b4397b352967e3213</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/ma3019014$$EPDF$$P50$$Gacs$$H</linktopdf><linktohtml>$$Uhttps://pubs.acs.org/doi/10.1021/ma3019014$$EHTML$$P50$$Gacs$$H</linktohtml><link.rule.ids>315,782,786,2769,27085,27933,27934,56747,56797</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=26751484$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>Zhang, Ning</creatorcontrib><creatorcontrib>Salzinger, Stephan</creatorcontrib><creatorcontrib>Rieger, Bernhard</creatorcontrib><title>Poly(vinylphosphonate)s with Widely Tunable LCST: A Promising Alternative to Conventional Thermoresponsive Polymers</title><title>Macromolecules</title><addtitle>Macromolecules</addtitle><description>Novel statistic copolymers of dialkyl vinylphosphonates have been synthesized via rare earth metal-mediated group transfer polymerization using easily accessible tris(cyclopentadienyl)ytterbium. The copolymerization parameters have been determined by activity measurements showing the formation of almost perfectly random copolymers (r 1, r 2 ∼ 1). Thus, the polymerization rate of vinylphosphonate GTP is mainly limited by the steric demand of growing polymer chain end. The obtained copolymers of diethyl vinylphosphonate and dimethyl or di-n-propyl vinylphosphonate show thermoresponsive properties, i.e., exhibit a tunable lower critical solution temperature following a coil–globule transition mechanism, with cloud points between 5 and 92 °C. Hereby, the LCST can be precisely adjusted by varying the comonomer composition and correlates linearly with the content of hydrophilic/hydrophobic comonomer. These thermoresponsive poly(vinylphosphonate)s, exhibiting a sharp and reversible phase transition, and minor environmental effects such as concentration and additives on their cloud point, are promising candidates in biomedical applications.</description><subject>Applied sciences</subject><subject>Copolymerization</subject><subject>Exact sciences and technology</subject><subject>Organic polymers</subject><subject>Physicochemistry of polymers</subject><subject>Preparation, kinetics, thermodynamics, mechanism and catalysts</subject><issn>0024-9297</issn><issn>1520-5835</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><recordid>eNptkEtLw0AUhQdRsFYX_oPZCHYRnUcy07grwRcULBhxGSbJjZ0ymQkzaSX_3pRKceHicrnwnXM5B6FrSu4oYfS-VZzQlND4BE1owkiUzHlyiiaEsDhKWSrP0UUIG0IoTWI-QWHlzHC703Yw3dqFcazqYRbwt-7X-FPXYAacb60qDeBl9p4_4AVeedfqoO0XXpge_KjQO8C9w5mzO7C9Hk0MztfgW-chdM6GPbB_1YIPl-isUSbA1e-eoo-nxzx7iZZvz6_ZYhkpzkQfNXwOtWgApKQKpOBNFctSlEIyBcBlyiUXDRsPUtcxEWXMU1nyhKVCAmeUT9Hs4Ft5F4KHpui8bpUfCkqKfVvFsa2RvTmwnQqVMo1XttLhKGBCJjSe_-FUFYqN247hTfjH7wc6-XcT</recordid><startdate>20121221</startdate><enddate>20121221</enddate><creator>Zhang, Ning</creator><creator>Salzinger, Stephan</creator><creator>Rieger, Bernhard</creator><general>American Chemical Society</general><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20121221</creationdate><title>Poly(vinylphosphonate)s with Widely Tunable LCST: A Promising Alternative to Conventional Thermoresponsive Polymers</title><author>Zhang, Ning ; Salzinger, Stephan ; Rieger, Bernhard</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a326t-f38ed6fee771ae763fc47b6b672aee3793736f22ae0dd406b4397b352967e3213</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Applied sciences</topic><topic>Copolymerization</topic><topic>Exact sciences and technology</topic><topic>Organic polymers</topic><topic>Physicochemistry of polymers</topic><topic>Preparation, kinetics, thermodynamics, mechanism and catalysts</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zhang, Ning</creatorcontrib><creatorcontrib>Salzinger, Stephan</creatorcontrib><creatorcontrib>Rieger, Bernhard</creatorcontrib><collection>Pascal-Francis</collection><collection>CrossRef</collection><jtitle>Macromolecules</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zhang, Ning</au><au>Salzinger, Stephan</au><au>Rieger, Bernhard</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Poly(vinylphosphonate)s with Widely Tunable LCST: A Promising Alternative to Conventional Thermoresponsive Polymers</atitle><jtitle>Macromolecules</jtitle><addtitle>Macromolecules</addtitle><date>2012-12-21</date><risdate>2012</risdate><volume>45</volume><issue>24</issue><spage>9751</spage><epage>9758</epage><pages>9751-9758</pages><issn>0024-9297</issn><eissn>1520-5835</eissn><coden>MAMOBX</coden><abstract>Novel statistic copolymers of dialkyl vinylphosphonates have been synthesized via rare earth metal-mediated group transfer polymerization using easily accessible tris(cyclopentadienyl)ytterbium. The copolymerization parameters have been determined by activity measurements showing the formation of almost perfectly random copolymers (r 1, r 2 ∼ 1). Thus, the polymerization rate of vinylphosphonate GTP is mainly limited by the steric demand of growing polymer chain end. The obtained copolymers of diethyl vinylphosphonate and dimethyl or di-n-propyl vinylphosphonate show thermoresponsive properties, i.e., exhibit a tunable lower critical solution temperature following a coil–globule transition mechanism, with cloud points between 5 and 92 °C. Hereby, the LCST can be precisely adjusted by varying the comonomer composition and correlates linearly with the content of hydrophilic/hydrophobic comonomer. These thermoresponsive poly(vinylphosphonate)s, exhibiting a sharp and reversible phase transition, and minor environmental effects such as concentration and additives on their cloud point, are promising candidates in biomedical applications.</abstract><cop>Washington, DC</cop><pub>American Chemical Society</pub><doi>10.1021/ma3019014</doi><tpages>8</tpages></addata></record> |
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subjects | Applied sciences Copolymerization Exact sciences and technology Organic polymers Physicochemistry of polymers Preparation, kinetics, thermodynamics, mechanism and catalysts |
title | Poly(vinylphosphonate)s with Widely Tunable LCST: A Promising Alternative to Conventional Thermoresponsive Polymers |
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