Please use this identifier to cite or link to this item: http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/6582
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dc.contributor.authorSHARMA, RASHMIen_US
dc.contributor.authorVIJAY, AMALen_US
dc.contributor.authorMUKHERJEE, ARNABen_US
dc.contributor.authorTALUKDAR, PINAKIen_US
dc.date.accessioned2022-02-18T05:26:14Z
dc.date.available2022-02-18T05:26:14Z
dc.date.issued2022-03en_US
dc.identifier.citationOrganic & Biomolecular Chemistry, 20(10), 2054-2058.en_US
dc.identifier.issn1477-0539en_US
dc.identifier.urihttps://doi.org/10.1039/D1OB02028Een_US
dc.identifier.urihttp://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/6582
dc.description.abstractWe report the development of supramolecular bis(cholyl) ion channels by using oxalamide and hydrazide as selectivity filters. The hydrazide system displayed superior chloride transport activity than oxalamide via the formation of a barrel stave channel. The better chloride recognition within the hydrazide channel over the oxalalmide was confirmed from the theoretical calculations.en_US
dc.language.isoenen_US
dc.publisherRoyal Society of Chemistryen_US
dc.subjectChemistryen_US
dc.subject2022-FEB-WEEK3en_US
dc.subjectTOC-FEB-2022en_US
dc.subject2022en_US
dc.titleBis(cholyl)-based chloride channels with oxalamide and hydrazide selectivity filtersen_US
dc.typeArticleen_US
dc.contributor.departmentDept. of Chemistryen_US
dc.identifier.sourcetitleOrganic & Biomolecular Chemistryen_US
dc.publication.originofpublisherForeignen_US
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