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Determining Chiral Configuration of Diamines via Contact Angle Measurements on Enantioselective Alanine-Appended Benzene-Tricarboxamide Gelators

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dc.contributor.authorJung, Sung Ho-
dc.contributor.authorKim, Ka Young-
dc.contributor.authorAhn, Ahreum-
dc.contributor.authorChoi, Myong Yong-
dc.contributor.authorJaworski, Justyn-
dc.contributor.authorJung, Jong Hwa-
dc.date.accessioned2025-10-14T08:30:13Z-
dc.date.available2025-10-14T08:30:13Z-
dc.date.issued2016-06-
dc.identifier.issn1944-8244-
dc.identifier.issn1944-8252-
dc.identifier.urihttps://scholarworks.gnu.ac.kr/handle/sw.gnu/80287-
dc.description.abstractSpectroscopic techniques exist that may discern between enantiomers and assess chiral purity. A nonspectroscopic approach that may be directly observed could provide numerous benefits. Using chiral alanine-appended benzene-tricarboxamide gelators, we reveal a methanol gel system that is capable of providing visual discrimination between enantiomers of various diamines. Specifically, gelation is induced by supramolecular nanofiber assembly resulting from interaction between a chiral gelator and a diamine of opposing chirality (i.e., a heterochiral system). Upon further implementing the chiral gelator in electrospun fibers as solid state films, we revealed enantioselective surface wetting properties that allowed for determining chirality through contact angle measurements. While these two approaches of observable gelation and surface wetting offer nonspectroscopic approaches, we also find that the supramolecular nanofiber assembly was able to enhance the induced circular dichroism signal resulting from addition of chiral diamines, allowing precise quantification of their enantiomeric purity.-
dc.format.extent7-
dc.language영어-
dc.language.isoENG-
dc.publisherAmerican Chemical Society-
dc.titleDetermining Chiral Configuration of Diamines via Contact Angle Measurements on Enantioselective Alanine-Appended Benzene-Tricarboxamide Gelators-
dc.typeArticle-
dc.publisher.location미국-
dc.identifier.doi10.1021/acsami.6b02611-
dc.identifier.scopusid2-s2.0-84974839112-
dc.identifier.wosid000377642100051-
dc.identifier.bibliographicCitationACS Applied Materials & Interfaces, v.8, no.22, pp 14102 - 14108-
dc.citation.titleACS Applied Materials & Interfaces-
dc.citation.volume8-
dc.citation.number22-
dc.citation.startPage14102-
dc.citation.endPage14108-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClasssci-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaScience & Technology - Other Topics-
dc.relation.journalResearchAreaMaterials Science-
dc.relation.journalWebOfScienceCategoryNanoscience & Nanotechnology-
dc.relation.journalWebOfScienceCategoryMaterials Science, Multidisciplinary-
dc.subject.keywordPlusENANTIOMERIC EXCESS-
dc.subject.keywordPlusNMR-SPECTROSCOPY-
dc.subject.keywordPlusCARBOXYLIC-ACIDS-
dc.subject.keywordPlusMETAL-COMPLEXES-
dc.subject.keywordPlusDISCRIMINATION-
dc.subject.keywordPlusRECOGNITION-
dc.subject.keywordPlusREAGENT-
dc.subject.keywordPlusRESOLUTION-
dc.subject.keywordPlusCOMPOUND-
dc.subject.keywordPlusPOLYMER-
dc.subject.keywordAuthorchiral configuration-
dc.subject.keywordAuthorenantiomer-
dc.subject.keywordAuthorelectrospun film-
dc.subject.keywordAuthorcontact angle-
dc.subject.keywordAuthorenantioselectivity-
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