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dc.contributor.authorLee, HFen_US
dc.contributor.authorSheu, HSen_US
dc.contributor.authorJeng, USen_US
dc.contributor.authorHuang, CFen_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/ma050254aen_US
dc.identifier.urihttp://hdl.handle.net/11536/13471-
dc.description.abstractWe have successfully prepared a new class of self-assembled biomaterial: a polypeptide-block-polypseudorotaxane diblock copolymer. This diblock copolymer is comprised of an a-helical polypeptide rod, based on gamma-benzyl-L-glutamate, and an originally coiled segment P(EO19-r-PO3); it forms inclusion complexes with a-cyclodextrins (alpha-CDs) to give crystalline polypseudorotaxanes. Formation of the polypseudorotaxane converts the conformation of P(EO19-r-PO3) from a flexible chain into a rodlike structure, which results in a novel block copolymer exhibiting a rod-rod conformation. Intrinsic interactions (e.g., the polypseudorotaxane's channel-type crystallization, the polypeptide's secondary structure, and microphase separation) within and between these rod-rod diblock copolymers contribute to their hierarchical self-assembly behavior, which we characterized using DSC, H-1 NMR spectroscopy, C-13 CP/MAS NMR spectroscopy, WAXS, and SAXS. The data obtained from the WAXS and SAXS studies clearly indicate the formation of juxtaposed bilayer-like nanostructure featuring hexagonally packed PBLG stacks and channel-type polypseudorotaxane moieties.en_US
dc.language.isoen_USen_US
dc.titlePreparation and supramolecular self-assembly of a polypeptide-block-polypseudorotaxaneen_US
dc.typeArticleen_US
dc.identifier.doi10.1021/ma050254aen_US
dc.identifier.journalMACROMOLECULESen_US
dc.citation.volume38en_US
dc.citation.issue15en_US
dc.citation.spage6551en_US
dc.citation.epage6558en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.identifier.wosnumberWOS:000230627000043-
dc.citation.woscount27-
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