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Selective Anion Exchange and Tunable Luminescent Behaviors of Metal–Organic Framework Based Supramolecular Isomers

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dc.contributor.author Manna, Biplab en_US
dc.contributor.author Singh, Shweta en_US
dc.contributor.author Karmakar, Avishek en_US
dc.contributor.author DESAI, AAMOD V. en_US
dc.contributor.author GHOSH, SUJIT K. en_US
dc.date.accessioned 2019-03-15T11:23:39Z
dc.date.available 2019-03-15T11:23:39Z
dc.date.issued 2015-01 en_US
dc.identifier.citation Inorganic Chemistry, 54 (1), 110-116. en_US
dc.identifier.issn 0020-1669 en_US
dc.identifier.issn 1520-510X en_US
dc.identifier.uri http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/2192
dc.identifier.uri https://doi.org/10.1021/ic501879w en_US
dc.description.abstract Owing to the conformational (cis or trans) flexibility of a N-donor ligand, the combinations of the same and Cd(ClO4)2 under variable solvent templates afforded two supramolecular isomers based on two-dimensional metal–organic frameworks. Both compounds contain weakly coordinating ClO4– anions attached to the metal centers. Both frameworks showed facile anion exchange behaviors with various kinds of foreign anions. Moreover, both frameworks showed anion-driven structural dynamism and exhibited the preferential uptake of strongly coordinating anions over others. Anion-regulated modulation in luminescent behaviors was also observed in both cases. en_US
dc.language.iso en en_US
dc.publisher American Chemical Society en_US
dc.subject Anion Exchange en_US
dc.subject Luminescent Behaviors en_US
dc.subject Supramolecular Isomers en_US
dc.subject Organic Framework en_US
dc.subject SEM images en_US
dc.subject 2015 en_US
dc.title Selective Anion Exchange and Tunable Luminescent Behaviors of Metal–Organic Framework Based Supramolecular Isomers en_US
dc.type Article en_US
dc.contributor.department Dept. of Chemistry en_US
dc.identifier.sourcetitle Inorganic Chemistry en_US
dc.publication.originofpublisher Foreign en_US


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