Synthesis, Properties, and Light-Induced Shape Memory Effect of Multiblock Polyesterurethanes Containing Biodegradable Segments and Pendant Cinnamamide Groups
Novel multiblock polyesterurethanes containing crystalline hard and amorphous soft segments and pendant cinnamamide moieties were designed and synthesized via a two-step polyaddition reaction using N,N-bis(2-hydroxyethyl) cinnamamide (BHECA), biodegradable poly(l,l-lactide) (PLLA), and poly(ε-caprol...
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Veröffentlicht in: | Biomacromolecules 2011-01, Vol.12 (1), p.235-241 |
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description | Novel multiblock polyesterurethanes containing crystalline hard and amorphous soft segments and pendant cinnamamide moieties were designed and synthesized via a two-step polyaddition reaction using N,N-bis(2-hydroxyethyl) cinnamamide (BHECA), biodegradable poly(l,l-lactide) (PLLA), and poly(ε-caprolactone) (PCL) diols as raw materials and hexamethylene diisocyanate (HDI) as coupling agent and characterized by 1H NMR, FTIR, UV, DSC, tensile and photomechanical tests, and so on. The copolymers behaved as typical thermoplastic elastomers and showed satisfactory thermal and mechanical properties. They also exhibited light-induced shape memory effect (LSME) at room temperature on exposure to light stimuli. The pendant cinnamamide groups work as photoresponsive molecular switches and provide the polymer with LSME via reversible [2 + 2] cycloaddition cross-linking. The strain fixity (R f) increases with the content of BHECA and the strain recovery (R r) increases with the content of PLLA. The R f reaches 50% at a BHECA content of 20 wt % and the R r reaches >95% at PLLA content of 50 wt %. |
doi_str_mv | 10.1021/bm1012162 |
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The copolymers behaved as typical thermoplastic elastomers and showed satisfactory thermal and mechanical properties. They also exhibited light-induced shape memory effect (LSME) at room temperature on exposure to light stimuli. The pendant cinnamamide groups work as photoresponsive molecular switches and provide the polymer with LSME via reversible [2 + 2] cycloaddition cross-linking. The strain fixity (R f) increases with the content of BHECA and the strain recovery (R r) increases with the content of PLLA. The R f reaches 50% at a BHECA content of 20 wt % and the R r reaches >95% at PLLA content of 50 wt %.</description><identifier>ISSN: 1525-7797</identifier><identifier>EISSN: 1526-4602</identifier><identifier>DOI: 10.1021/bm1012162</identifier><identifier>PMID: 21125994</identifier><language>eng</language><publisher>Washington, DC: American Chemical Society</publisher><subject>Applied sciences ; Cinnamates - chemistry ; Exact sciences and technology ; Lactic Acid - chemistry ; Organic polymers ; Photochemistry - methods ; Physicochemistry of polymers ; Polyesters - chemical synthesis ; Polyesters - chemistry ; Polymers - chemistry ; Polymers with particular properties ; Polyurethanes - chemical synthesis ; Polyurethanes - chemistry ; Preparation, kinetics, thermodynamics, mechanism and catalysts</subject><ispartof>Biomacromolecules, 2011-01, Vol.12 (1), p.235-241</ispartof><rights>Copyright © 2010 American Chemical Society</rights><rights>2015 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a410t-70b6f3398d5147f0a7704bb53610c3209dbd14d344d1eed3cc3f5c9dc9e099553</citedby><cites>FETCH-LOGICAL-a410t-70b6f3398d5147f0a7704bb53610c3209dbd14d344d1eed3cc3f5c9dc9e099553</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/bm1012162$$EPDF$$P50$$Gacs$$H</linktopdf><linktohtml>$$Uhttps://pubs.acs.org/doi/10.1021/bm1012162$$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=23740629$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21125994$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wu, Linbo</creatorcontrib><creatorcontrib>Jin, Chunli</creatorcontrib><creatorcontrib>Sun, Xiangying</creatorcontrib><title>Synthesis, Properties, and Light-Induced Shape Memory Effect of Multiblock Polyesterurethanes Containing Biodegradable Segments and Pendant Cinnamamide Groups</title><title>Biomacromolecules</title><addtitle>Biomacromolecules</addtitle><description>Novel multiblock polyesterurethanes containing crystalline hard and amorphous soft segments and pendant cinnamamide moieties were designed and synthesized via a two-step polyaddition reaction using N,N-bis(2-hydroxyethyl) cinnamamide (BHECA), biodegradable poly(l,l-lactide) (PLLA), and poly(ε-caprolactone) (PCL) diols as raw materials and hexamethylene diisocyanate (HDI) as coupling agent and characterized by 1H NMR, FTIR, UV, DSC, tensile and photomechanical tests, and so on. The copolymers behaved as typical thermoplastic elastomers and showed satisfactory thermal and mechanical properties. They also exhibited light-induced shape memory effect (LSME) at room temperature on exposure to light stimuli. The pendant cinnamamide groups work as photoresponsive molecular switches and provide the polymer with LSME via reversible [2 + 2] cycloaddition cross-linking. The strain fixity (R f) increases with the content of BHECA and the strain recovery (R r) increases with the content of PLLA. The R f reaches 50% at a BHECA content of 20 wt % and the R r reaches >95% at PLLA content of 50 wt %.</description><subject>Applied sciences</subject><subject>Cinnamates - chemistry</subject><subject>Exact sciences and technology</subject><subject>Lactic Acid - chemistry</subject><subject>Organic polymers</subject><subject>Photochemistry - methods</subject><subject>Physicochemistry of polymers</subject><subject>Polyesters - chemical synthesis</subject><subject>Polyesters - chemistry</subject><subject>Polymers - chemistry</subject><subject>Polymers with particular properties</subject><subject>Polyurethanes - chemical synthesis</subject><subject>Polyurethanes - chemistry</subject><subject>Preparation, kinetics, thermodynamics, mechanism and catalysts</subject><issn>1525-7797</issn><issn>1526-4602</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNptkc1u1DAUhSNERUthwQsgbxCqRIp_4_ESRqWtNFVHGlhHjn0945LYqe0s5mV41oZ2aDes7ll8Okfn3Kr6QPA5wZR87QaCCSUNfVWdEEGbmjeYvn7UopZSyePqbc53GGPFuHhTHVNCqFCKn1R_NvtQdpB9_oLWKY6QiodZ62DRym93pb4OdjJg0WanR0A3MMS0RxfOgSkoOnQz9cV3fTS_0Tr2e8gF0pSg7HSAjJYxFO2DD1v03UcL26St7npAG9gOEEp-DFpDsDoUtPQh6EEP3gK6THEa87vqyOk-w_vDPa1-_bj4ubyqV7eX18tvq1pzgkstcdc4xtTCCsKlw1pKzLtOsIZgwyhWtrOEW8a5JQCWGcOcMMoaBVgpIdhp9fnJd0zxfppLtIPPBvp-bhGn3C6YIESIhZzJsyfSpJhzAteOyQ867VuC27_faJ-_MbMfD65TN4B9Jv_NPwOfDoDORvcu6WB8fuGY5Lih6oXTJrd3cUphHuM_gQ8a8J-V</recordid><startdate>20110110</startdate><enddate>20110110</enddate><creator>Wu, Linbo</creator><creator>Jin, Chunli</creator><creator>Sun, Xiangying</creator><general>American Chemical Society</general><scope>IQODW</scope><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></search><sort><creationdate>20110110</creationdate><title>Synthesis, Properties, and Light-Induced Shape Memory Effect of Multiblock Polyesterurethanes Containing Biodegradable Segments and Pendant Cinnamamide Groups</title><author>Wu, Linbo ; Jin, Chunli ; Sun, Xiangying</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a410t-70b6f3398d5147f0a7704bb53610c3209dbd14d344d1eed3cc3f5c9dc9e099553</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Applied sciences</topic><topic>Cinnamates - chemistry</topic><topic>Exact sciences and technology</topic><topic>Lactic Acid - chemistry</topic><topic>Organic polymers</topic><topic>Photochemistry - methods</topic><topic>Physicochemistry of polymers</topic><topic>Polyesters - chemical synthesis</topic><topic>Polyesters - chemistry</topic><topic>Polymers - chemistry</topic><topic>Polymers with particular properties</topic><topic>Polyurethanes - chemical synthesis</topic><topic>Polyurethanes - chemistry</topic><topic>Preparation, kinetics, thermodynamics, mechanism and catalysts</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wu, Linbo</creatorcontrib><creatorcontrib>Jin, Chunli</creatorcontrib><creatorcontrib>Sun, Xiangying</creatorcontrib><collection>Pascal-Francis</collection><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><jtitle>Biomacromolecules</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wu, Linbo</au><au>Jin, Chunli</au><au>Sun, Xiangying</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Synthesis, Properties, and Light-Induced Shape Memory Effect of Multiblock Polyesterurethanes Containing Biodegradable Segments and Pendant Cinnamamide Groups</atitle><jtitle>Biomacromolecules</jtitle><addtitle>Biomacromolecules</addtitle><date>2011-01-10</date><risdate>2011</risdate><volume>12</volume><issue>1</issue><spage>235</spage><epage>241</epage><pages>235-241</pages><issn>1525-7797</issn><eissn>1526-4602</eissn><abstract>Novel multiblock polyesterurethanes containing crystalline hard and amorphous soft segments and pendant cinnamamide moieties were designed and synthesized via a two-step polyaddition reaction using N,N-bis(2-hydroxyethyl) cinnamamide (BHECA), biodegradable poly(l,l-lactide) (PLLA), and poly(ε-caprolactone) (PCL) diols as raw materials and hexamethylene diisocyanate (HDI) as coupling agent and characterized by 1H NMR, FTIR, UV, DSC, tensile and photomechanical tests, and so on. The copolymers behaved as typical thermoplastic elastomers and showed satisfactory thermal and mechanical properties. They also exhibited light-induced shape memory effect (LSME) at room temperature on exposure to light stimuli. The pendant cinnamamide groups work as photoresponsive molecular switches and provide the polymer with LSME via reversible [2 + 2] cycloaddition cross-linking. The strain fixity (R f) increases with the content of BHECA and the strain recovery (R r) increases with the content of PLLA. The R f reaches 50% at a BHECA content of 20 wt % and the R r reaches >95% at PLLA content of 50 wt %.</abstract><cop>Washington, DC</cop><pub>American Chemical Society</pub><pmid>21125994</pmid><doi>10.1021/bm1012162</doi><tpages>7</tpages></addata></record> |
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subjects | Applied sciences Cinnamates - chemistry Exact sciences and technology Lactic Acid - chemistry Organic polymers Photochemistry - methods Physicochemistry of polymers Polyesters - chemical synthesis Polyesters - chemistry Polymers - chemistry Polymers with particular properties Polyurethanes - chemical synthesis Polyurethanes - chemistry Preparation, kinetics, thermodynamics, mechanism and catalysts |
title | Synthesis, Properties, and Light-Induced Shape Memory Effect of Multiblock Polyesterurethanes Containing Biodegradable Segments and Pendant Cinnamamide Groups |
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