Alignment of helical nanofilaments on the surfaces of various self-assembled monolayers

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dc.contributor.authorKim, Hanimko
dc.contributor.authorLee, Sunheeko
dc.contributor.authorShin, Tae Jooko
dc.contributor.authorCha, Yun Jeongko
dc.contributor.authorKorblova, Evako
dc.contributor.authorWalba, David M.ko
dc.contributor.authorClark, Noel A.ko
dc.contributor.authorLee, Sang Bokko
dc.contributor.authorYoon, Dong Kiko
dc.date.accessioned2013-08-08T05:02:03Z-
dc.date.available2013-08-08T05:02:03Z-
dc.date.created2013-07-16-
dc.date.created2013-07-16-
dc.date.issued2013-
dc.identifier.citationSOFT MATTER, v.9, no.26, pp.6185 - 6191-
dc.identifier.issn1744-683X-
dc.identifier.urihttp://hdl.handle.net/10203/174369-
dc.description.abstractWe successfully prepared controlled layers of NOBOW molecules on a variety of self-assembled monolayers (SAMs) such that the layers formed oriented domain structures in which the complex chiral/polar crystalline helical nanofilaments (HNFs) were arranged to form a B4 bent-core liquid crystal (LC) phase. The alignment of the B2 phase, which formed at a higher temperature than the B4 phase, affected the direction of the HNFs. The HNFs formed on the B2 smectic layers and were aligned parallel or perpendicular, respectively, to the substrates with high or low surface energies (molecule-philic or -phobic SAM-treated substrates). The HNFs confined within rectangular microchannels modified by the SAMs were directly visualized by electron microscopy and X-ray diffraction studies. The orientations of the HNFs were found to be governed by the B2 smectic layer morphology.-
dc.languageEnglish-
dc.publisherROYAL SOC CHEMISTRY-
dc.subjectLIQUID-CRYSTAL PHASE-
dc.subjectACHIRAL MOLECULES-
dc.subjectCONFINEMENT-
dc.subjectGEOMETRY-
dc.subjectDOMAINS-
dc.subjectMESOGEN-
dc.titleAlignment of helical nanofilaments on the surfaces of various self-assembled monolayers-
dc.typeArticle-
dc.identifier.wosid000320270400018-
dc.identifier.scopusid2-s2.0-84881077470-
dc.type.rimsART-
dc.citation.volume9-
dc.citation.issue26-
dc.citation.beginningpage6185-
dc.citation.endingpage6191-
dc.citation.publicationnameSOFT MATTER-
dc.identifier.doi10.1039/c3sm50637a-
dc.contributor.localauthorYoon, Dong Ki-
dc.contributor.nonIdAuthorKim, Hanim-
dc.contributor.nonIdAuthorLee, Sunhee-
dc.contributor.nonIdAuthorShin, Tae Joo-
dc.contributor.nonIdAuthorCha, Yun Jeong-
dc.contributor.nonIdAuthorKorblova, Eva-
dc.contributor.nonIdAuthorWalba, David M.-
dc.contributor.nonIdAuthorClark, Noel A.-
dc.type.journalArticleArticle-
dc.subject.keywordPlusLIQUID-CRYSTAL PHASE-
dc.subject.keywordPlusACHIRAL MOLECULES-
dc.subject.keywordPlusCONFINEMENT-
dc.subject.keywordPlusGEOMETRY-
dc.subject.keywordPlusDOMAINS-
dc.subject.keywordPlusMESOGEN-
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