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dc.contributor.authorKuo, Shiao-Weien_US
dc.contributor.authorTung, Pao-Hsaingen_US
dc.contributor.authorLai, Chih-Lingen_US
dc.contributor.authorJeong, Kwang-Unen_US
dc.contributor.authorChang, Feng-Chihen_US
dc.date.accessioned2014-12-08T15:12:39Z-
dc.date.available2014-12-08T15:12:39Z-
dc.date.issued2008-02-01en_US
dc.identifier.issn1022-1336en_US
dc.identifier.urihttp://dx.doi.org/10.1002/marc.200700697en_US
dc.identifier.urihttp://hdl.handle.net/11536/9721-
dc.description.abstractThis paper describes a new approach towards preparing self-assembled hydrogen-bonded complexes that have vesicle and patched spherical structures from two species of block copolymer in non-selective solvents. The assembly of vesicles from the intermolecular complex formed after mixing polystyrene-block-poly(4-vinyl phenol) (PS-b-PVPh) with poly(methyl methacrylate)-block-poly(4-vinylpyridine) (PMMA-b-P4VP) in tetrahydrofuran (THF) is driven by strong hydrogen bonding between the complementary binding sites on the PVPh and P4VP blocks. In contrast, well-defined patched spherical micelles form after blending PS-b-PVPh with weaker hydrogen bonds form between the PVPh and P4VP blocks in DMF, relative to those in THF, which results in the formation of spherical micelles that have compartmentalized coronas that consist of PS and PMMA blocks.en_US
dc.language.isoen_USen_US
dc.subjectblock copolymersen_US
dc.subjecthydrogen bondingen_US
dc.subjectpolymer complexesen_US
dc.subjectself-assemblyen_US
dc.subjectseparated coilsen_US
dc.titleSupramolecular micellization of diblock copolymer mixtures mediated by hydrogen bonding for the observation of separated coil and chain aggregation in common solventsen_US
dc.typeArticleen_US
dc.identifier.doi10.1002/marc.200700697en_US
dc.identifier.journalMACROMOLECULAR RAPID COMMUNICATIONSen_US
dc.citation.volume29en_US
dc.citation.issue3en_US
dc.citation.spage229en_US
dc.citation.epage233en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.identifier.wosnumberWOS:000253332600019-
dc.citation.woscount28-
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