Please use this identifier to cite or link to this item: http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/2097
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dc.contributor.authorSaha, Tanmoyen_US
dc.contributor.authorRoy, Arundhatien_US
dc.contributor.authorGening, Marina L.en_US
dc.contributor.authorTitov, Denis V.en_US
dc.contributor.authorGerbst, Alexey G.en_US
dc.contributor.authorTsvetkov, Yury E.en_US
dc.contributor.authorNifantiev, Nikolay E.en_US
dc.contributor.authorTALUKDAR, PINAKIen_US
dc.date.accessioned2019-02-25T09:26:08Z
dc.date.available2019-02-25T09:26:08Z
dc.date.issued2014-03en_US
dc.identifier.citationChemical Communications, 50(41), 5514-5516.en_US
dc.identifier.issn1359-7345en_US
dc.identifier.issn1364-548Xen_US
dc.identifier.urihttp://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/2097-
dc.identifier.urihttps://doi.org/10.1039/C3CC49490Jen_US
dc.description.abstractUnimolecular ion channels were designed by functionalization of a new type of cyclic oligosaccharides, cyclo-oligo-(1 → 6)-β-D-glucosamines, with pentabutylene glycol chains. Their ion transporting activity was tuned by varying oligomericity. A halide selectivity sequence, Cl− > Br− > I− was observed.en_US
dc.language.isoenen_US
dc.publisherRoyal Society of Chemistryen_US
dc.subjectCyclo-oligoen_US
dc.subjectD-glucosamineen_US
dc.subjectArtificial channelsen_US
dc.subjectTransmembrane ion transporten_US
dc.subjectCyclic oligosaccharidesen_US
dc.subject2014en_US
dc.titleCyclo-oligo-(1 → 6)-β-d-glucosamine based artificial channels for tunable transmembrane ion transporten_US
dc.typeArticleen_US
dc.contributor.departmentDept. of Chemistryen_US
dc.identifier.sourcetitleChemical Communicationsen_US
dc.publication.originofpublisherForeignen_US
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