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dc.contributor.authorShinde, Sopan Valibaen_US
dc.contributor.authorTALUKDAR, PINAKIen_US
dc.date.accessioned2018-10-05T03:34:02Z
dc.date.available2018-10-05T03:34:02Z
dc.date.issued2018-08en_US
dc.identifier.citationChemical Communications. Vol.54(73), 10351-10354.en_US
dc.identifier.issn1364-548Xen_US
dc.identifier.urihttp://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/1201
dc.identifier.urihttps://doi.org/10.1039/C8CC04044Cen_US
dc.description.abstractIndole-based amide-sulfonamide derivatives were synthesized. The X-ray crystal structure and chloride binding studies in solution showed a 1 : 1 stoichiometry. The ion transport efficiency directly correlated to the pKa of the sulfonamide N–H protons. The mechanistic study indicated proton–anion symport across the lipid bilayer membrane.en_US
dc.language.isoenen_US
dc.publisherRoyal Society of Chemistryen_US
dc.subjectChemistryen_US
dc.subjectTOC-SEP-2018en_US
dc.subject2018en_US
dc.titleAn anion receptor that facilitates transmembrane proton–anion symport by deprotonating its sulfonamide N–H protonen_US
dc.typeArticleen_US
dc.contributor.departmentDept. of Chemistryen_US
dc.identifier.sourcetitleChemical Communicationsen_US
dc.publication.originofpublisherForeignen_US
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