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Foldecture as a Core Material with Anisotropic Surface Characteristics

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dc.contributor.authorYoo, Sung Hyun-
dc.contributor.authorEom, Taedaehyeong-
dc.contributor.authorKwon, Sunbum-
dc.contributor.authorGong, Jintaek-
dc.contributor.authorKim, Jin-
dc.contributor.authorCho, Sung June-
dc.contributor.authorDriver, Russell W.-
dc.contributor.authorLee, Yunho-
dc.contributor.authorKim, Hyungjun-
dc.contributor.authorLee, Hee-Seung-
dc.date.accessioned2022-05-13T03:40:12Z-
dc.date.available2022-05-13T03:40:12Z-
dc.date.issued2015-02-
dc.identifier.issn0002-7863-
dc.identifier.issn1520-5126-
dc.identifier.urihttps://scholarworks.bwise.kr/cau/handle/2019.sw.cau/57632-
dc.description.abstractThe synthesis of microscale, polyhedrally shaped, soft materials with anisotropic surface functionality by a bottom-up approach remains a significant challenge. Herein we report a microscale molecular architecture (foldecture) with facet-dependent surface characteristics that can potentially serve as a well-defined catalytic template. Rhombic rod shaped foldectures with six facets were obtained by the aqueous self-assembly of helical beta-peptide foldamers with a C-terminal carboxylic acid. An analysis of the molecular packing by X-ray diffraction revealed that carboxylic acid groups were exposed exclusively on the two (001) rhombic facets due to antiparallel packing of the helical peptides. A surface energy calculation by molecular dynamics simulation was performed to provide a plausible explanation for the development of anisotropy during foldecture formation. The expected facet-selective surface properties of the foldecture were experimentally confirmed by selective deposition of metal nanoparticles on the (001) facets, leading to a new class of sequentially constructed, heterogeneous foldecture core materials.-
dc.format.extent4-
dc.language영어-
dc.language.isoENG-
dc.publisherAMER CHEMICAL SOC-
dc.titleFoldecture as a Core Material with Anisotropic Surface Characteristics-
dc.typeArticle-
dc.identifier.doi10.1021/ja510840v-
dc.identifier.bibliographicCitationJOURNAL OF THE AMERICAN CHEMICAL SOCIETY, v.137, no.6, pp 2159 - 2162-
dc.description.isOpenAccessN-
dc.identifier.wosid000349807000003-
dc.identifier.scopusid2-s2.0-84923260924-
dc.citation.endPage2162-
dc.citation.number6-
dc.citation.startPage2159-
dc.citation.titleJOURNAL OF THE AMERICAN CHEMICAL SOCIETY-
dc.citation.volume137-
dc.type.docTypeArticle-
dc.publisher.location미국-
dc.subject.keywordPlusBETA-PEPTIDE FOLDAMER-
dc.subject.keywordPlusGOLD NANOPARTICLES-
dc.subject.keywordPlusMOLECULAR-DYNAMICS-
dc.subject.keywordPlusCRYSTALS-
dc.subject.keywordPlusARCHITECTURES-
dc.subject.keywordPlusSIMULATIONS-
dc.subject.keywordPlusNANOTUBES-
dc.subject.keywordPlusPROTEINS-
dc.subject.keywordPlusDESIGN-
dc.subject.keywordPlusGROWTH-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalWebOfScienceCategoryChemistry, Multidisciplinary-
dc.description.journalRegisteredClasssci-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
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