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Manifesting Subtle Differences of Neutral Hydrophilic Guest Isomers in a Molecular Container by Phase Transfer

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dc.contributor.authorLee, Hyun Hee L.-
dc.contributor.authorLee, Jong Wha-
dc.contributor.authorJang, Yoonjung-
dc.contributor.authorKo, Young Ho-
dc.contributor.authorKim, Kimoon-
dc.contributor.authorKim, Hugh I.-
dc.date.accessioned2021-09-03T21:58:51Z-
dc.date.available2021-09-03T21:58:51Z-
dc.date.created2021-06-18-
dc.date.issued2016-07-11-
dc.identifier.issn1433-7851-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/88073-
dc.description.abstractAchieving strong host-guest interactions between synthetic hosts and hydrophilic guests in solution is challenging because solvation effects overwhelm other effects. To resolve this issue, we transferred complexes of cucurbit[7]uril (CB[7]) and monosaccharides to the gas phase and report here their intrinsic host-guest chemistry in the absence of solvation effects. It was observed that effective host-guest interactions in the gas phase mediated by ammonium cations allow the differentiation of the monosaccharide isomers in complex with CB[7] upon vibrational excitation. The potential of the unique observation was extended to a quantitative supramolecular analytical method for the monosaccharide guests. The combination of host-guest chemistry and phase transfer presented in this study is an effective approach to overcome current limitations in supramolecular chemistry.-
dc.languageEnglish-
dc.language.isoen-
dc.publisherWILEY-V C H VERLAG GMBH-
dc.subjectIONIZATION MASS-SPECTROMETRY-
dc.subjectHIGH-AFFINITY BINDING-
dc.subjectGAS-PHASE-
dc.subjectSUPRAMOLECULAR CHEMISTRY-
dc.subjectCOLLISIONAL ACTIVATION-
dc.subjectNONCOVALENT COMPLEXES-
dc.subjectGLUCOSE BIOSENSORS-
dc.subjectRECOGNITION-
dc.subjectHOST-
dc.subjectAMINO-
dc.titleManifesting Subtle Differences of Neutral Hydrophilic Guest Isomers in a Molecular Container by Phase Transfer-
dc.typeArticle-
dc.contributor.affiliatedAuthorKim, Hugh I.-
dc.identifier.doi10.1002/anie.201601320-
dc.identifier.scopusid2-s2.0-84971393452-
dc.identifier.wosid000383253300007-
dc.identifier.bibliographicCitationANGEWANDTE CHEMIE-INTERNATIONAL EDITION, v.55, no.29, pp.8249 - 8253-
dc.relation.isPartOfANGEWANDTE CHEMIE-INTERNATIONAL EDITION-
dc.citation.titleANGEWANDTE CHEMIE-INTERNATIONAL EDITION-
dc.citation.volume55-
dc.citation.number29-
dc.citation.startPage8249-
dc.citation.endPage8253-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalWebOfScienceCategoryChemistry, Multidisciplinary-
dc.subject.keywordPlusIONIZATION MASS-SPECTROMETRY-
dc.subject.keywordPlusHIGH-AFFINITY BINDING-
dc.subject.keywordPlusGAS-PHASE-
dc.subject.keywordPlusSUPRAMOLECULAR CHEMISTRY-
dc.subject.keywordPlusCOLLISIONAL ACTIVATION-
dc.subject.keywordPlusNONCOVALENT COMPLEXES-
dc.subject.keywordPlusGLUCOSE BIOSENSORS-
dc.subject.keywordPlusRECOGNITION-
dc.subject.keywordPlusHOST-
dc.subject.keywordPlusAMINO-
dc.subject.keywordAuthorcucurbit[7]uril-
dc.subject.keywordAuthorgas-phase chemistry-
dc.subject.keywordAuthorhost-guest systems-
dc.subject.keywordAuthormass spectrometry-
dc.subject.keywordAuthormonosaccharides-
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