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http://dspace.bits-pilani.ac.in:8080/jspui/xmlui/handle/123456789/3362Full metadata record
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Sakhuja, Rajeev | - |
| dc.contributor.author | Pant, Debi D. | - |
| dc.date.accessioned | 2021-11-11T10:59:54Z | - |
| dc.date.available | 2021-11-11T10:59:54Z | - |
| dc.date.issued | 2016-08-27 | - |
| dc.identifier.uri | https://link.springer.com/article/10.1007%2Fs10895-016-1913-1 | - |
| dc.identifier.uri | http://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/3362 | - |
| dc.description.abstract | A coumarin-indole dyad, N-((7-hydroxy-2-oxo-2H-chromen-4-yl)methyl)-1H-indole-2-carboxamide has been synthesized and characterized by 1H-NMR and 13C-NMR. Effect of various metal ions on fluorescent behavior was also studied. The synthesized compound showed remarkable specificity towards Li+ in organo-aqueous medium over other metal ions. Coordination of the compound with Li+ induces a turn-on fluorescence response. The sensor exhibited good binding constant and low detection limit towards Li+. Experimental results have been verified with Density Functional Theory and Time Dependent Density Functional Theory calculations. | en_US |
| dc.language.iso | en | en_US |
| dc.publisher | Springer | en_US |
| dc.subject | Chemistry | en_US |
| dc.subject | H2O/CH3CN | en_US |
| dc.subject | Coumarin-Indole | en_US |
| dc.title | Highly Selective Sensing of Li+ in H2O/CH3CN via Fluorescence ‘Turn-on’ Response of a Coumarin-Indole Linked Dyad: an Experimental and Theoretical Study | en_US |
| dc.type | Article | en_US |
| Appears in Collections: | Department of Chemistry | |
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