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Cited 806 time in webofscience Cited 846 time in scopus
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dc.contributor.authorKim, K-
dc.contributor.authorSelvapalam, N-
dc.contributor.authorKo, YH-
dc.contributor.authorPark, KM-
dc.contributor.authorKim, D-
dc.contributor.authorKim, J-
dc.date.accessioned2015-06-25T01:46:31Z-
dc.date.available2015-06-25T01:46:31Z-
dc.date.created2009-02-28-
dc.date.issued2007-01-
dc.identifier.issn0306-0012-
dc.identifier.other2015-OAK-0000006564en_US
dc.identifier.urihttps://oasis.postech.ac.kr/handle/2014.oak/10045-
dc.description.abstractCucurbit[n]uril (CB[n], n = 5-10), a new family of molecular hosts comprising n glycoluril units, have gained much attention in the new millennium for their exceptional molecular recognition ability. The CB homologues have brought dynamism to CB chemistry, as witnessed by the heightened interest in the field for the last several years. Compared to the chemistry of cyclodextrins and calixarenes, however, that of CB[n] has developed slowly until recently, which may be attributed mainly to their poor solubility in common solvents, and inability to functionalize these molecules. The direct functionalization method of CB[n] propelled CB chemistry to a new height as this new method not only solved the solubility problem but also opened up the gateway to the generation of tailor-made CB[n] derivatives. The functionalization of CB [n] led us to investigate numerous applications including artificial ion channels, vesicles, stationary phases in chromatography, ISEs, polymers, nanomaterials, and many others. This tutorial review describes the recent advances and challenges in the functionalization of CBs along with the applications of functionalized CBs.-
dc.description.statementofresponsibilityopenen_US
dc.languageEnglish-
dc.publisherROYAL SOC CHEMISTRY-
dc.relation.isPartOfCHEMICAL SOCIETY REVIEWS-
dc.rightsBY_NC_NDen_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/2.0/kren_US
dc.titleFunctionalized cucurbiturils and their applications-
dc.typeArticle-
dc.contributor.college화학과en_US
dc.identifier.doi10.1039/B603088M-
dc.author.googleKim, Ken_US
dc.author.googleSelvapalam, Nen_US
dc.author.googleKim, Jen_US
dc.author.googleKim, Den_US
dc.author.googlePark, KMen_US
dc.author.googleKo, YHen_US
dc.relation.volume36en_US
dc.relation.issue2en_US
dc.relation.startpage267en_US
dc.relation.lastpage279en_US
dc.contributor.id10104366en_US
dc.relation.journalCHEMICAL SOCIETY REVIEWSen_US
dc.relation.indexSCI급, SCOPUS 등재논문en_US
dc.relation.sciSCIen_US
dc.collections.nameJournal Papersen_US
dc.type.rimsART-
dc.identifier.bibliographicCitationCHEMICAL SOCIETY REVIEWS, v.36, no.2, pp.267 - 279-
dc.identifier.wosid000243841400014-
dc.date.tcdate2019-01-01-
dc.citation.endPage279-
dc.citation.number2-
dc.citation.startPage267-
dc.citation.titleCHEMICAL SOCIETY REVIEWS-
dc.citation.volume36-
dc.contributor.affiliatedAuthorKim, K-
dc.identifier.scopusid2-s2.0-33846669779-
dc.description.journalClass1-
dc.description.journalClass1-
dc.description.wostc587-
dc.description.scptc618*
dc.date.scptcdate2018-10-274*
dc.type.docTypeReview-
dc.subject.keywordPlusDERIVATIVES-
dc.subject.keywordPlusHOMOLOGS-
dc.subject.keywordPlusFACILE-
dc.subject.keywordPlusFAMILY-
dc.subject.keywordPlusHOST-
dc.subject.keywordPlusPHOTODIMERIZATION-
dc.subject.keywordPlusCHROMATOGRAPHY-
dc.subject.keywordPlusENCAPSULATION-
dc.subject.keywordPlusCOMPLEXATION-
dc.subject.keywordPlusSELECTIVITY-
dc.relation.journalWebOfScienceCategoryChemistry, Multidisciplinary-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaChemistry-

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김기문KIM, KIMOON
Dept of Chemistry
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