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Solid State and Solution Self-Assembly of Helical Polypeptides Tethered to Polyhedral Oligomeric Silsesquioxanes

dc.citation.epage1626en_US
dc.citation.issue5en_US
dc.citation.spage1619en_US
dc.citation.volume42en_US
dc.citation.woscount64
dc.contributor.authorKuo, Shiao-Weien_US
dc.contributor.authorLee, Hsin-Fangen_US
dc.contributor.authorHuang, Wu-Jangen_US
dc.contributor.authorJeong, Kwang-Unen_US
dc.contributor.authorChang, Feng-Chihen_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.date.accessioned2014-12-08T15:09:47Z
dc.date.available2014-12-08T15:09:47Z
dc.date.issued2009-03-10en_US
dc.description.abstractNew macromolecular self-assembling building blocks, polyhedral oligo- silsesquioxane (POSS)-helical polypeptide copolymers, have been synthesized through the ring-opening polymerization (ROP) of gamma-benzyl-L-glutamate N-carboxyanhydride (gamma-Bn-Glu NCA) using aminopropyl isobutyl-POSS as a macroinitiator. The incorporation of POSS units at the chain ends of PBLG moieties has two important effects: allowing intramolecular hydrogen bonding between the POSS and PBLG units to enhance the latter's a-helical conformations in the solid state and preventing the aggregation of nanoribbons through the POSS blocks' protrusion from the ribbons to allow the formation of clear gels in solution.en_US
dc.identifier.doi10.1021/ma802370yen_US
dc.identifier.issn0024-9297en_US
dc.identifier.journalMACROMOLECULESen_US
dc.identifier.urihttp://dx.doi.org/10.1021/ma802370yen_US
dc.identifier.urihttps://ir.lib.nycu.edu.tw/handle/11536/7493
dc.identifier.wosnumberWOS:000263883000033
dc.language.isoen_USen_US
dc.titleSolid State and Solution Self-Assembly of Helical Polypeptides Tethered to Polyhedral Oligomeric Silsesquioxanesen_US
dc.typeArticleen_US

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