Please use this identifier to cite or link to this item: http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/6346
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dc.contributor.authorAHMAD, MANZOORen_US
dc.contributor.authorCHATTOPADHAYAY, SANDIPen_US
dc.contributor.authorMONDAL, DEBASHISen_US
dc.contributor.authorVijayakanth, Thangavelen_US
dc.contributor.authorTALUKDAR, PINAKIen_US
dc.date.accessioned2021-11-01T04:13:56Z
dc.date.available2021-11-01T04:13:56Z
dc.date.issued2021-10en_US
dc.identifier.citationOrganic Letters, 23(19), 7319–7324.en_US
dc.identifier.issn1523-7060en_US
dc.identifier.issn1523-7052en_US
dc.identifier.urihttp://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/6346
dc.identifier.urihttps://doi.org/10.1021/acs.orglett.1c02249en_US
dc.description.abstractPhotoswitchable acylhydrazone-based synthetic anionophores are reported. Single-crystal X-ray structure and 1H NMR titration studies confirmed the chloride binding in solid and solution states. The ion transport activity of 1a was greatly attenuated through a phototriggered E to Z photoisomerization process, and the photoisomerized deactivated state showed high kinetic stability due to an intramolecular hydrogen bond. Switchable “OFF–ON” transport activity was achieved by the application of light and acid-catalyzed reactivation process.en_US
dc.language.isoenen_US
dc.publisherAmerican Chemical Societyen_US
dc.subjectArtificial Ion Channelsen_US
dc.subjectChloride Transporten_US
dc.subjectPotassium Channelsen_US
dc.subjectApoptosisen_US
dc.subjectAssembliesen_US
dc.subjectMoleculesen_US
dc.subjectEfficienten_US
dc.subjectSwitchesen_US
dc.subjectDynamicsen_US
dc.subjectPyridylen_US
dc.subject2021-OCT-WEEK3en_US
dc.subjectTOC-OCT-2021en_US
dc.subject2021en_US
dc.titleStimuli-Responsive Anion Transport through Acylhydrazone-Based Synthetic Anionophoresen_US
dc.typeArticleen_US
dc.contributor.departmentDept. of Chemistryen_US
dc.identifier.sourcetitleOrganic Lettersen_US
dc.publication.originofpublisherForeignen_US
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