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Recognition, Sensing, and Trapping of Bicarbonate Anions with a Dicationic meso-Bis(benzimidazolium) Calix[4]pyrrole

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dc.contributor.authorMulugeta, Endale-
dc.contributor.authorHe, Qing-
dc.contributor.authorSareen, Divya-
dc.contributor.authorHong, Seong-Jin-
dc.contributor.authorOh, Ju Hyun-
dc.contributor.authorLynch, Vincent M.-
dc.contributor.authorSessler, Jonathan L.-
dc.contributor.authorKim, Sung Kuk-
dc.contributor.authorLee, Chang-Hee-
dc.date.accessioned2022-12-26T18:19:08Z-
dc.date.available2022-12-26T18:19:08Z-
dc.date.issued2017-12-14-
dc.identifier.issn2451-9294-
dc.identifier.urihttps://scholarworks.gnu.ac.kr/handle/sw.gnu/13275-
dc.description.abstractA meso-aryl calix[4]pyrrole derivative bearing benzimidazolium groups at the two diametrical meso positions was synthesized. The receptor acts as an effective host for the bicarbonate anion at concentrations as low as 4 nM. A change in fluorescence response was observed under conditions of fluorescence dye displacement when this functionalized calix[4]pyrrole was exposed to the HCO3- anion. Tests with various carbonated drinks revealed its ability to function as an easy-to-use sensor for dissolved CO2, as monitored through the bicarbonate anion concentration. Depending on the specific choice of conditions, recrystallization of the calix[4]pyrrole receptor in the presence of Cs2CO3 and methanol yielded crystals of either the HCO3- anion complex or methyl carbonate (CH3OCO2-), a normally difficult-to-access species whose formation under non-forcing equilibrium conditions is ascribed to trapping by the calix[4]pyrrole receptor. The present system thus provides a recognition-based approach to the chemical capture of hydrated, anionic forms of CO2.-
dc.format.extent13-
dc.language영어-
dc.language.isoENG-
dc.publisherCELL PRESS-
dc.titleRecognition, Sensing, and Trapping of Bicarbonate Anions with a Dicationic meso-Bis(benzimidazolium) Calix[4]pyrrole-
dc.typeArticle-
dc.publisher.location미국-
dc.identifier.doi10.1016/j.chempr.2017.10.007-
dc.identifier.scopusid2-s2.0-85038224307-
dc.identifier.wosid000418335800012-
dc.identifier.bibliographicCitationCHEM, v.3, no.6, pp 1008 - 1020-
dc.citation.titleCHEM-
dc.citation.volume3-
dc.citation.number6-
dc.citation.startPage1008-
dc.citation.endPage1020-
dc.type.docTypeArticle-
dc.description.isOpenAccessY-
dc.description.journalRegisteredClassscopus-
dc.description.journalRegisteredClassesci-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalWebOfScienceCategoryChemistry, Multidisciplinary-
dc.subject.keywordPlusSOLUBLE ADENYLYL-CYCLASE-
dc.subject.keywordPlusCARBON-DIOXIDE SENSORS-
dc.subject.keywordPlusIONIC LIQUIDS-
dc.subject.keywordPlusPHYSIOLOGICAL ROLES-
dc.subject.keywordPlusDIMETHYL CARBONATE-
dc.subject.keywordPlusDISSOLVED CO2-
dc.subject.keywordPlusCHEMOSENSOR-
dc.subject.keywordPlusFLUORESCENT-
dc.subject.keywordPlusTRANSPORT-
dc.subject.keywordPlusRECEPTOR-
dc.subject.keywordAuthorbicarbonate-
dc.subject.keywordAuthorCalix[4]pyrrole-
dc.subject.keywordAuthorcarbon dioxide-
dc.subject.keywordAuthorconversion-
dc.subject.keywordAuthormethyl carbonate-
dc.subject.keywordAuthorsensor-
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