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dc.contributor.authorHuang, Cheng-Weien_US
dc.contributor.authorWu, Pei-Weien_US
dc.contributor.authorSu, Wei-Hungen_US
dc.contributor.authorZhu, Chao-Yuanen_US
dc.contributor.authorKuo, Shiao-Weien_US
dc.date.accessioned2017-04-21T06:55:49Z-
dc.date.available2017-04-21T06:55:49Z-
dc.date.issued2016en_US
dc.identifier.issn1759-9954en_US
dc.identifier.urihttp://dx.doi.org/10.1039/c5py01852hen_US
dc.identifier.urihttp://hdl.handle.net/11536/133403-
dc.description.abstractA new homopolymer of polystyrene (PS) presenting pendant diaminopyridine (DAP) moieties has been prepared using controlled free radical polymerization and a CuAAC "click" reaction. Through directional complementary multiple hydrogen bonding, this PVB-DAP polymer underwent complexation with a thymine-functionalized azobenzene (Azo-T). The resulting supramolecular complex exhibited amorphous and chromophoric behavior without microphase separation. This strategy allowed the fabrication of homogeneous stimuli-responsive thin films with photocontrollable behavior through photoinduced trans-cis isomerization. The PVB-DAP/Azo-T supramolecular complex facilitated the dispersion of an azo-dye through noncovalent interactions; the resulting complex was used to fabricate a surface relief grating displaying an interference pattern. The "recordability" and "rewritability" of these supramolecular complexes suggest that they are promising materials for optical applications and therefore advance the pathway for supramolecular development.en_US
dc.language.isoen_USen_US
dc.titleStimuli-responsive supramolecular materials: photo-tunable properties and molecular recognition behavioren_US
dc.identifier.doi10.1039/c5py01852hen_US
dc.identifier.journalPOLYMER CHEMISTRYen_US
dc.citation.volume7en_US
dc.citation.issue4en_US
dc.citation.spage795en_US
dc.citation.epage806en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.identifier.wosnumberWOS:000368895700006en_US
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