Please use this identifier to cite or link to this item: https://doi.org/10.1021/ma8009646
DC FieldValue
dc.titlePseudo-block copolymer based on star-shaped poly(N-isopropylacrylamide) with a β-cyclodextrin core and guest-bearing PEG: Controlling thermoresponsivity through supramolecular self-assembly
dc.contributor.authorZhang, Z.-X.
dc.contributor.authorLiu, X.
dc.contributor.authorXu, F.J.
dc.contributor.authorLoh, X.J.
dc.contributor.authorKang, E.-T.
dc.contributor.authorNeon, K.-G.
dc.contributor.authorLi, J.
dc.date.accessioned2014-04-25T09:05:13Z
dc.date.available2014-04-25T09:05:13Z
dc.date.issued2008-08-26
dc.identifier.citationZhang, Z.-X., Liu, X., Xu, F.J., Loh, X.J., Kang, E.-T., Neon, K.-G., Li, J. (2008-08-26). Pseudo-block copolymer based on star-shaped poly(N-isopropylacrylamide) with a β-cyclodextrin core and guest-bearing PEG: Controlling thermoresponsivity through supramolecular self-assembly. Macromolecules 41 (16) : 5967-5970. ScholarBank@NUS Repository. https://doi.org/10.1021/ma8009646
dc.identifier.issn00249297
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/51812
dc.description.abstractA study was conducted to control thermoresponsivity with supramolecular self-assembly of pseudo-block copolymer based on star-shaped poly(N-isopropylacrylamide) with a β-cyclodextrin core and guest-bearing PEG. The study used a star polymer, synthesized with a β-CD core as molecular recognition moiety and multiple PNIPAAm arms as actuation moieties. Nuclear magnetic resonance (NMR) spectroscopy and X-ray photoelectron spectroscopy (XPS) were used to determine the degree of substitution (DS) of the purified macroinitiator. The study found that β-CD-core star polymer was obtained by synthesis of a β-CD-based macroinitiator. The study synthesized the macromolecular guests by coupling the molecular recognition moiety, adamantane with biocompatible hydrophilic poly(ehtylene glycol) (PEG).
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1021/ma8009646
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentBIOENGINEERING
dc.contributor.departmentCHEMICAL & BIOMOLECULAR ENGINEERING
dc.description.doi10.1021/ma8009646
dc.description.sourcetitleMacromolecules
dc.description.volume41
dc.description.issue16
dc.description.page5967-5970
dc.description.codenMAMOB
dc.identifier.isiut000258580700004
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