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  ETC 1. Journal Papers

 

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dc.contributor.authorKim, SK-
dc.contributor.authorSingh, NJ-
dc.contributor.authorKim, SJ-
dc.contributor.authorSwamy, KMK-
dc.contributor.authorKim, SH-
dc.contributor.authorLee, KH-
dc.contributor.authorKim, KS-
dc.contributor.authorYoon, J-
dc.date.accessioned2016-04-01T02:11:30Z-
dc.date.available2016-04-01T02:11:30Z-
dc.date.created2009-03-20-
dc.date.issued2005-05-09-
dc.identifier.issn0040-4020-
dc.identifier.other2005-OAK-0000005077-
dc.identifier.urihttps://oasis.postech.ac.kr/handle/2014.oak/24621-
dc.description.abstractFor the recognition and sensing of anionic analytes, comparative studies were carried out on the anion bindings of pyrophosphate, H2PO4-, and dicarboxylates to the anthracene derivatives bearing two urea groups on the 1,8 and 9, 10-positions as fluorescent chemosensors for anions. Their binding properties were compared using fluorescence and H-1 NMR, and the results were rationalized with an ab initio study. (c) 2005 Elsevier Ltd. All rights reserved.-
dc.description.statementofresponsibilityX-
dc.languageEnglish-
dc.publisherPERGAMON-ELSEVIER SCIENCE LTD-
dc.relation.isPartOfTETRAHEDRON-
dc.subjectfluorescence-
dc.subjectfluorescence chemosensor-
dc.subjectanion-
dc.subjectanion-receptor-
dc.subjectpyrophosphate-
dc.subjectadipate-
dc.subjectdicarboxylates-
dc.subjectmolecular recognition-
dc.subjectAQUEOUS-SOLUTION-
dc.subjectARTIFICIAL RECEPTORS-
dc.subjectCHEMOSENSORS-
dc.subjectRECOGNITION-
dc.subjectSENSORS-
dc.subjectPYROPHOSPHATE-
dc.subjectCOMPLEXATION-
dc.subjectHYDROGEN-
dc.subjectBINDING-
dc.subjectSPACER-
dc.titleAnthracene derivatives bearing two urea groups as fluorescent receptors for anions-
dc.typeArticle-
dc.contributor.college화학과-
dc.identifier.doi10.1016/J.TET.2005.0-
dc.author.googleKim, SK-
dc.author.googleSingh, NJ-
dc.author.googleKim, SJ-
dc.author.googleSwamy, KMK-
dc.author.googleKim, SH-
dc.author.googleLee, KH-
dc.author.googleKim, KS-
dc.author.googleYoon, J-
dc.relation.volume61-
dc.relation.issue19-
dc.relation.startpage4545-
dc.relation.lastpage4550-
dc.contributor.id10051563-
dc.relation.journalTETRAHEDRON-
dc.relation.indexSCI급, SCOPUS 등재논문-
dc.relation.sciSCI-
dc.collections.nameJournal Papers-
dc.type.rimsART-
dc.identifier.bibliographicCitationTETRAHEDRON, v.61, no.19, pp.4545 - 4550-
dc.identifier.wosid000228768000003-
dc.date.tcdate2019-02-01-
dc.citation.endPage4550-
dc.citation.number19-
dc.citation.startPage4545-
dc.citation.titleTETRAHEDRON-
dc.citation.volume61-
dc.contributor.affiliatedAuthorKim, KS-
dc.description.journalClass1-
dc.description.journalClass1-
dc.description.wostc90-
dc.type.docTypeArticle-
dc.subject.keywordPlusAQUEOUS-SOLUTION-
dc.subject.keywordPlusRECOGNITION-
dc.subject.keywordPlusCHEMOSENSORS-
dc.subject.keywordPlusPYROPHOSPHATE-
dc.subject.keywordPlusHYDROGEN-
dc.subject.keywordPlusBINDING-
dc.subject.keywordAuthorfluorescence-
dc.subject.keywordAuthorfluorescence chemosensor-
dc.subject.keywordAuthoranion-
dc.subject.keywordAuthoranion-receptor-
dc.subject.keywordAuthorpyrophosphate-
dc.subject.keywordAuthoradipate-
dc.subject.keywordAuthordicarboxylates-
dc.subject.keywordAuthormolecular recognition-
dc.relation.journalWebOfScienceCategoryChemistry, Organic-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaChemistry-
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