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A calix[4]pyrrole functionalized with an amidoindole ester for the selective recognition of the dihydrogen phosphate anion

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dc.contributor.authorOh, Ju Hyun-
dc.contributor.authorShin, Sang Kyu-
dc.contributor.authorKim, Sung Kuk-
dc.date.accessioned2025-09-04T06:30:19Z-
dc.date.available2025-09-04T06:30:19Z-
dc.date.issued2025-08-
dc.identifier.issn1359-7345-
dc.identifier.issn1364-548X-
dc.identifier.urihttps://scholarworks.gnu.ac.kr/handle/sw.gnu/79761-
dc.description.abstractA bisamidoindole ester-functionalized calix[4]pyrrole (2), which features additional hydrogen bond donors and acceptors, complexes dihydrogen phosphate (H2PO4-) with high affinity and selectivity. This binding takes place via distinct modes compared to those observed for meso-pyrrolic calix[4]pyrrole 1 and the parent calix[4]pyrrole, underscoring the impact of strategic functionalization on anion binding geometry and selectivity.-
dc.format.extent4-
dc.language영어-
dc.language.isoENG-
dc.publisherRoyal Society of Chemistry-
dc.titleA calix[4]pyrrole functionalized with an amidoindole ester for the selective recognition of the dihydrogen phosphate anion-
dc.typeArticle-
dc.publisher.location영국-
dc.identifier.doi10.1039/d5cc03617h-
dc.identifier.scopusid2-s2.0-105014325711-
dc.identifier.wosid001544477500001-
dc.identifier.bibliographicCitationChemical Communications, v.61, no.71, pp 13425 - 13428-
dc.citation.titleChemical Communications-
dc.citation.volume61-
dc.citation.number71-
dc.citation.startPage13425-
dc.citation.endPage13428-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalWebOfScienceCategoryChemistry, Multidisciplinary-
dc.subject.keywordPlusRECEPTORS-
dc.subject.keywordPlusBINDING-
dc.subject.keywordPlusDESIGN-
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