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dc.contributor.authorLin, CLen_US
dc.contributor.authorChen, WCen_US
dc.contributor.authorLiao, CSen_US
dc.contributor.authorSu, YCen_US
dc.contributor.authorHuang, CFen_US
dc.contributor.authorKuo, SWen_US
dc.contributor.authorChang, FCen_US
dc.date.accessioned2014-12-08T15:18:44Z-
dc.date.available2014-12-08T15:18:44Z-
dc.date.issued2005-07-26en_US
dc.identifier.issn0024-9297en_US
dc.identifier.urihttp://dx.doi.org/10.1021/ma050639ten_US
dc.identifier.urihttp://hdl.handle.net/11536/13470-
dc.description.abstractA series of poly(vinylphenol-co-methyl methacrylate) (PVPh-co-PMMA) block and random copolymers were prepared through anionic and free radical polymerizations, respectively, of 4-tert-butoxystyrene and methyl methacrylate and subsequent selective hydrolysis of the 4-tert-butoxystyrene protective groups. Analysis of infrared spectra suggests that the random copolymer possesses a higher fraction of hydrogen-bonded carbonyl groups and a larger interassociation equilibrium constant relative to those of a block copolymer containing similar vinylphenol content because of the different sequence distribution that may arise from the so-called intramolecular screening effect. In contrast, the glass transition temperature of the block copolymer, which has the lower polydispersity index, is higher than that of the random copolymer at the same composition.en_US
dc.language.isoen_USen_US
dc.titleSequence distribution and polydispersity index affect the hydrogen-bonding strength of poly(vinylphenol-co-methyl methacrylate) copolymersen_US
dc.typeArticleen_US
dc.identifier.doi10.1021/ma050639ten_US
dc.identifier.journalMACROMOLECULESen_US
dc.citation.volume38en_US
dc.citation.issue15en_US
dc.citation.spage6435en_US
dc.citation.epage6444en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.identifier.wosnumberWOS:000230627000030-
dc.citation.woscount39-
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