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Cited 25 time in webofscience Cited 24 time in scopus
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dc.contributor.authorNumata, M-
dc.contributor.authorSugiyasu, K-
dc.contributor.authorKishida, T-
dc.contributor.authorHaraguchi, S-
dc.contributor.authorFujita, N-
dc.contributor.authorPark, SM-
dc.contributor.authorYun, YJ-
dc.contributor.authorKim, BH-
dc.contributor.authorShinkai, S-
dc.date.accessioned2015-06-25T02:55:03Z-
dc.date.available2015-06-25T02:55:03Z-
dc.date.created2009-03-19-
dc.date.issued2008-01-
dc.identifier.issn1477-0520-
dc.identifier.other2015-OAK-0000007493en_US
dc.identifier.urihttps://oasis.postech.ac.kr/handle/2014.oak/11875-
dc.description.abstractThe influence of added polynucleotide on the gelation ability of nucleobase-appended organogelators was investigated. Uracil-appended cholesterol gelator formed a stable organogel in polar organic solvents such as n-butanol. It was found that the addition of the complementary polyadenylic acid (poly(A)) not only stabilizes the gel but also creates the helical structure in the original gel phase. Thymidine and thymine-appended gelators can form stable gel in apolar solvents, such as benzene, where poly(A)-lipid complex can act as a complementary template for the gelator molecules to create the fibrous composites. Based on these findings, we can conclude that self-assembling modes and gelation properties of nucleobase-appended organogelators are controllable by the addition of their complementary polynucleotide in organic solvents. We believe, therefore, that the present system can open the new paths to accelerate development of well-controlled one-dimensional molecular assembly systems, which would be indispensable for the creation of novel nanomaterials based on organic compounds.-
dc.description.statementofresponsibilityopenen_US
dc.languageEnglish-
dc.publisherROYAL SOC CHEMISTRY-
dc.relation.isPartOfORGANIC & BIOMOLECULAR CHEMISTRY-
dc.rightsBY_NC_NDen_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/2.0/kren_US
dc.titleCreation of polynucleotide-assisted molecular assemblies in organic solvents: general strategy toward the creation of artificial DNA-like nanoarchitectures-
dc.typeArticle-
dc.contributor.college화학과en_US
dc.identifier.doi10.1039/B713354E-
dc.author.googleNumata, Men_US
dc.author.googleSugiyasu, Ken_US
dc.author.googleShinkai, Sen_US
dc.author.googleKim, BHen_US
dc.author.googleYun, YJen_US
dc.author.googlePark, SMen_US
dc.author.googleFujita, Nen_US
dc.author.googleHaraguchi, Sen_US
dc.author.googleKishida, Ten_US
dc.relation.volume6en_US
dc.relation.issue4en_US
dc.relation.startpage712en_US
dc.relation.lastpage718en_US
dc.contributor.id10142056en_US
dc.relation.journalORGANIC & BIOMOLECULAR CHEMISTRYen_US
dc.relation.indexSCI급, SCOPUS 등재논문en_US
dc.relation.sciSCIen_US
dc.collections.nameJournal Papersen_US
dc.type.rimsART-
dc.identifier.bibliographicCitationORGANIC & BIOMOLECULAR CHEMISTRY, v.6, no.4, pp.712 - 718-
dc.identifier.wosid000253014900010-
dc.date.tcdate2019-01-01-
dc.citation.endPage718-
dc.citation.number4-
dc.citation.startPage712-
dc.citation.titleORGANIC & BIOMOLECULAR CHEMISTRY-
dc.citation.volume6-
dc.contributor.affiliatedAuthorKim, BH-
dc.identifier.scopusid2-s2.0-38949155160-
dc.description.journalClass1-
dc.description.journalClass1-
dc.description.wostc21-
dc.description.scptc19*
dc.date.scptcdate2018-10-274*
dc.type.docTypeArticle-
dc.subject.keywordPlusGEL-
dc.subject.keywordPlusGELATION-
dc.subject.keywordPlusORGANOGEL-
dc.subject.keywordPlusGELATORS-
dc.subject.keywordPlusTRANSCRIPTION-
dc.subject.keywordPlusWATER-
dc.relation.journalWebOfScienceCategoryChemistry, Organic-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaChemistry-

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김병현KIM, BYEANG HYEAN
Div of Advanced Materials Science
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