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dc.contributor.authorKuo, Shiao-Weien_US
dc.contributor.authorHong, Jing-Longen_US
dc.contributor.authorHuang, Yu-Chanen_US
dc.contributor.authorChen, Jem-Kunen_US
dc.contributor.authorFan, Shih-Kangen_US
dc.contributor.authorKo, Fu-Hsiangen_US
dc.contributor.authorChu, Chih-Weien_US
dc.contributor.authorChang, Feng-Chihen_US
dc.date.accessioned2014-12-08T15:23:44Z-
dc.date.available2014-12-08T15:23:44Z-
dc.date.issued2012en_US
dc.identifier.issn1687-4110en_US
dc.identifier.urihttp://hdl.handle.net/11536/16560-
dc.identifier.urihttp://dx.doi.org/749732en_US
dc.description.abstractNew star poly(N-isopropylacrylamide)-b-polyhedral oligomeric silsesquioxane (PNIPAm-b-POSS) copolymers were synthesized from octa-azido functionalized POSS (N-3-POSS) and alkyne-PNIPAm, which was prepared using an alkyne-functionalized atom transfer radical polymerization (ATRP) initiator (propargyl 2-bromo-2-methylpropionamide), via click chemistry. These star PNIPAm-b-POSS copolymers undergo a sharp coil-globule transition in water at above 32 degrees C changing from a hydrophilic state below this temperature to a hydrophobic state above it, which is similar to linear PNIPAm homopolymers. More interestingly, we found that these star polymers exhibited strong blue photoluminescence in water above a lower critical solution temperature (LCST). This photoluminescence was likely due to the constrained geometric freedom and relatively rigid structure caused by intramolecular hydrogen bonding within the star PNIPAm polymers, which exhibit an intrinsic fluorescent behavior.en_US
dc.language.isoen_USen_US
dc.titleStar Poly(N-isopropylacrylamide) Tethered to Polyhedral Oligomeric Silsesquioxane (POSS) Nanoparticles by a Combination of ATRP and Click Chemistryen_US
dc.typeArticleen_US
dc.identifier.doi749732en_US
dc.identifier.journalJOURNAL OF NANOMATERIALSen_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.identifier.wosnumberWOS:000306057700001-
dc.citation.woscount4-
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