{"@context":{"@vocab":"https://cir.nii.ac.jp/schema/1.0/","rdfs":"http://www.w3.org/2000/01/rdf-schema#","dc":"http://purl.org/dc/elements/1.1/","dcterms":"http://purl.org/dc/terms/","foaf":"http://xmlns.com/foaf/0.1/","prism":"http://prismstandard.org/namespaces/basic/2.0/","cinii":"http://ci.nii.ac.jp/ns/1.0/","datacite":"https://schema.datacite.org/meta/kernel-4/","ndl":"http://ndl.go.jp/dcndl/terms/","jpcoar":"https://github.com/JPCOAR/schema/blob/master/2.0/"},"@id":"https://cir.nii.ac.jp/crid/1361981470339873152.json","@type":"Article","productIdentifier":[{"identifier":{"@type":"DOI","@value":"10.1002/pola.28879"}},{"identifier":{"@type":"URI","@value":"https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2Fpola.28879"}},{"identifier":{"@type":"URI","@value":"https://onlinelibrary.wiley.com/doi/pdf/10.1002/pola.28879"}}],"dc:title":[{"@value":"Designing catechol‐end functionalized poly(DMAm‐<i>co</i>‐NIPAM) by RAFT with tunable LCSTs"}],"description":[{"type":"abstract","notation":[{"@value":"<jats:title>ABSTRACT</jats:title><jats:p>Providing catechol‐end functionality to controlled structure lower critical solution temperature (LCST) copolymers is attractive, given the versatility of catechol chemistry for tethering to nanostructures. Controlled polymer chain lengths with catechol RAFT end groups are of interest to provide tunable LCST behavior to nanoparticles, although these polymerizations are relatively unexplored. Herein, the reactivity ratios for the RAFT copolymerization of <jats:italic>N,N</jats:italic>‐dimethylacrylamide (DMAm) and <jats:italic>N</jats:italic>‐isopropylacrylamide (NIPAM) pairs based on catechol‐end RAFT agents using an <jats:italic>in situ</jats:italic> NMR technique were first determined. Several catechol‐end poly(DMAm‐<jats:italic>co</jats:italic>‐NIPAM) samples were then prepared using the RAFT agent to provide copolymer. The reactivity ratios for the DMAm‐NIPAM pair were <jats:italic>r</jats:italic><jats:sub>DMAm</jats:sub> = 1.28–1.31 and <jats:italic>r</jats:italic><jats:sub>NIPAM</jats:sub> = 0.48–0.51. All the poly(DMAm‐<jats:italic>co</jats:italic>‐NIPAM) samples were found to have <jats:italic>M</jats:italic><jats:sub>n</jats:sub> values ≤ 26 kDa and <jats:italic>Ð</jats:italic> < 1.08 with LCST values ranging from 31 to 92°C, while maintaining a short range of glass transition temperature (<jats:italic>T</jats:italic><jats:sub>g</jats:sub> = 118–137°C). The difference in LCST values for the catechol functionalized poly(DMAm‐<jats:italic>co</jats:italic>‐NIPAM) based on 0.5 wt% aqueous buffered solutions at pH 5.5 and 8.5 was found to be <3.0°C. These conditions are suitable for subsequent catechol‐induced coordination and nucleophilic addition chemistry for covalent and noncovalent linkages during subsequent post‐modification. © 2017 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. <jats:bold>2017</jats:bold>, <jats:italic>55</jats:italic>, 4062–4070</jats:p>"}]}],"creator":[{"@id":"https://cir.nii.ac.jp/crid/1381981470339873024","@type":"Researcher","foaf:name":[{"@value":"Olabode O. Oyeneye"}],"jpcoar:affiliationName":[{"@value":"Department of Chemical and Biochemical Engineering University of Western Ontario London ON N6A‐5B9 Canada"}]},{"@id":"https://cir.nii.ac.jp/crid/1381981470339873152","@type":"Researcher","foaf:name":[{"@value":"William Z. Xu"}],"jpcoar:affiliationName":[{"@value":"Department of Chemical and Biochemical Engineering University of Western Ontario London ON N6A‐5B9 Canada"}]},{"@id":"https://cir.nii.ac.jp/crid/1381981470339873153","@type":"Researcher","foaf:name":[{"@value":"Paul A. Charpentier"}],"jpcoar:affiliationName":[{"@value":"Department of Chemical and Biochemical Engineering University of Western Ontario London ON N6A‐5B9 Canada"}]}],"publication":{"publicationIdentifier":[{"@type":"PISSN","@value":"0887624X"},{"@type":"EISSN","@value":"10990518"}],"prism:publicationName":[{"@value":"Journal of Polymer Science Part A: Polymer Chemistry"}],"dc:publisher":[{"@value":"Wiley"}],"prism:publicationDate":"2017-10-15","prism:volume":"55","prism:number":"24","prism:startingPage":"4062","prism:endingPage":"4070"},"reviewed":"false","dc:rights":["http://onlinelibrary.wiley.com/termsAndConditions#vor"],"url":[{"@id":"https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2Fpola.28879"},{"@id":"https://onlinelibrary.wiley.com/doi/pdf/10.1002/pola.28879"}],"createdAt":"2017-10-15","modifiedAt":"2023-10-05","relatedProduct":[{"@id":"https://cir.nii.ac.jp/crid/1390564238108800512","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@language":"en","@value":"Retardation Effect of Catechol Moiety during Radical Copolymerization of 3,4-Dihydroxystyrene with Various Monomers"}]}],"dataSourceIdentifier":[{"@type":"CROSSREF","@value":"10.1002/pola.28879"},{"@type":"CROSSREF","@value":"10.1246/cl.190305_references_DOI_UXYmdnXSMM6csudgyrqOIspLexJ"}]}