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Cited 280 time in webofscience Cited 288 time in scopus
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dc.contributor.authorIhm, H-
dc.contributor.authorYun, S-
dc.contributor.authorKim, HG-
dc.contributor.authorKim, JK-
dc.contributor.authorKim, KS-
dc.date.accessioned2016-03-31T13:02:25Z-
dc.date.available2016-03-31T13:02:25Z-
dc.date.created2009-02-28-
dc.date.issued2002-08-22-
dc.identifier.issn1523-7060-
dc.identifier.other2002-OAK-0000002853-
dc.identifier.urihttps://oasis.postech.ac.kr/handle/2014.oak/18933-
dc.description.abstract[GRAPHIC] A positively charged tripodal receptor with nitro groups in the imidazolium rings was designed, synthesized, and characterized for its anion binding strength. The receptor shows strong affinity and high selectivity for Cl- through (C-H)(+)---X- hydrogen bonds wherein charge-charge and charge-dipole electrostatic interactions dominate. The association constant with chloride anion in a 9:1 mixture of acetonitrile-d(3) and DMSO-d(6) is measured to be 1.1 x 10(6) M-1. The receptor also shows reasonably high affinity toward H2PO4-.-
dc.description.statementofresponsibilityX-
dc.languageEnglish-
dc.publisherAMER CHEMICAL SOC-
dc.relation.isPartOfORGANIC LETTERS-
dc.subjectCATION-PI INTERACTIONS-
dc.subjectSYNTHETIC RECEPTOR-
dc.subjectSELECTIVITY-
dc.subjectCHEMISTRY-
dc.subjectCONSTANTS-
dc.subjectBENZENE-
dc.subjectDESIGN-
dc.subjectORIGIN-
dc.titleTripodal nitro-imidazolium receptor for anion binding driven by (C-H)(+)-X- hydrogen bonds-
dc.typeArticle-
dc.contributor.college화학과-
dc.identifier.doi10.1021/OL026373H-
dc.author.googleIhm, H-
dc.author.googleYun, S-
dc.author.googleKim, HG-
dc.author.googleKim, JK-
dc.author.googleKim, KS-
dc.relation.volume4-
dc.relation.issue17-
dc.relation.startpage2897-
dc.relation.lastpage2900-
dc.contributor.id10051563-
dc.relation.journalORGANIC LETTERS-
dc.relation.indexSCI급, SCOPUS 등재논문-
dc.relation.sciSCI-
dc.collections.nameJournal Papers-
dc.type.rimsART-
dc.identifier.bibliographicCitationORGANIC LETTERS, v.4, no.17, pp.2897 - 2900-
dc.identifier.wosid000177617000023-
dc.date.tcdate2019-01-01-
dc.citation.endPage2900-
dc.citation.number17-
dc.citation.startPage2897-
dc.citation.titleORGANIC LETTERS-
dc.citation.volume4-
dc.contributor.affiliatedAuthorKim, KS-
dc.identifier.scopusid2-s2.0-0000811579-
dc.description.journalClass1-
dc.description.journalClass1-
dc.description.wostc251-
dc.description.scptc250*
dc.date.scptcdate2018-05-121*
dc.type.docTypeArticle-
dc.subject.keywordPlusCATION-PI INTERACTIONS-
dc.subject.keywordPlusSYNTHETIC RECEPTOR-
dc.subject.keywordPlusSELECTIVITY-
dc.subject.keywordPlusCHEMISTRY-
dc.subject.keywordPlusCONSTANTS-
dc.subject.keywordPlusBENZENE-
dc.subject.keywordPlusDESIGN-
dc.subject.keywordPlusORIGIN-
dc.relation.journalWebOfScienceCategoryChemistry, Organic-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaChemistry-

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