Cyclo-oligo-(1 → 6)-β-d-glucosamine based artificial channels for tunable transmembrane ion transport

Roy, Arundhati; Gerbst, Alexey G.; Nifantiev, Nikolay E.; Tsvetkov, Yury E.; Gening, Marina L.; Saha, Tanmoy; Titov, Denis V.; TALUKDAR, PINAKI

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dc.contributor.author	Saha, Tanmoy	en_US
dc.contributor.author	Roy, Arundhati	en_US
dc.contributor.author	Gening, Marina L.	en_US
dc.contributor.author	Titov, Denis V.	en_US
dc.contributor.author	Gerbst, Alexey G.	en_US
dc.contributor.author	Tsvetkov, Yury E.	en_US
dc.contributor.author	Nifantiev, Nikolay E.	en_US
dc.contributor.author	TALUKDAR, PINAKI	en_US
dc.date.accessioned	2019-02-25T09:26:08Z
dc.date.available	2019-02-25T09:26:08Z
dc.date.issued	2014-03	en_US
dc.identifier.citation	Chemical Communications, 50(41), 5514-5516.	en_US
dc.identifier.issn	1359-7345	en_US
dc.identifier.issn	1364-548X	en_US
dc.identifier.uri	http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/2097
dc.identifier.uri	https://doi.org/10.1039/C3CC49490J	en_US
dc.description.abstract	Unimolecular 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.iso	en	en_US
dc.publisher	Royal Society of Chemistry	en_US
dc.subject	Cyclo-oligo	en_US
dc.subject	D-glucosamine	en_US
dc.subject	Artificial channels	en_US
dc.subject	Transmembrane ion transport	en_US
dc.subject	Cyclic oligosaccharides	en_US
dc.subject	2014	en_US
dc.title	Cyclo-oligo-(1 → 6)-β-d-glucosamine based artificial channels for tunable transmembrane ion transport	en_US
dc.type	Article	en_US
dc.contributor.department	Dept. of Chemistry	en_US
dc.identifier.sourcetitle	Chemical Communications	en_US
dc.publication.originofpublisher	Foreign	en_US