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 |