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dc.contributor.authorIn, S-
dc.contributor.authorCho, SJ-
dc.contributor.authorKang, JM-
dc.date.accessioned2024-01-21T04:32:30Z-
dc.date.available2024-01-21T04:32:30Z-
dc.date.created2021-09-03-
dc.date.issued2005-09-
dc.identifier.issn1061-0278-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/136177-
dc.description.abstractA m-xylene bridged imidazolium receptor I has been designed and synthesized. The receptor 1 utilizes two imidazole (C-H)(+)-anion hydrogen bonds and one aromatic hydrogen-anion hydrogen bond. The major driving force of complexation between the receptor 1 and anions comes from two imidazole (C-H)(+)-anion hydrogen bonding. However, some hydrogen bonding energy between aromatic hydrogen and anion exists, although it is expected to be much smaller than that of imidazole (C-H)(+)-anion hydrogen bonds.-
dc.languageEnglish-
dc.publisherTAYLOR & FRANCIS LTD-
dc.subjectRECOGNITION-
dc.subjectHIGHLIGHTS-
dc.subjectHYDROGEN-
dc.titleAnion receptor with xylene bridged two imidazolium rings-
dc.typeArticle-
dc.identifier.doi10.1080/10610270500142468-
dc.description.journalClass1-
dc.identifier.bibliographicCitationSUPRAMOLECULAR CHEMISTRY, v.17, no.6, pp.443 - 446-
dc.citation.titleSUPRAMOLECULAR CHEMISTRY-
dc.citation.volume17-
dc.citation.number6-
dc.citation.startPage443-
dc.citation.endPage446-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid000232855200003-
dc.identifier.scopusid2-s2.0-27344461029-
dc.relation.journalWebOfScienceCategoryChemistry, Multidisciplinary-
dc.relation.journalResearchAreaChemistry-
dc.type.docTypeArticle-
dc.subject.keywordPlusRECOGNITION-
dc.subject.keywordPlusHIGHLIGHTS-
dc.subject.keywordPlusHYDROGEN-
dc.subject.keywordAuthoranion receptor-
dc.subject.keywordAuthoraromatic hydrogen bond-
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KIST Article > 2005
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