
Please use this identifier to cite or link to this item:
http://hdl.handle.net/123456789/2312
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DC Field | Value | Language |
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dc.contributor.author | Yadav, H.R. | - |
dc.contributor.author | Choudhury, A.R. | - |
dc.date.accessioned | 2020-11-27T05:45:37Z | - |
dc.date.available | 2020-11-27T05:45:37Z | - |
dc.date.issued | 2018 | - |
dc.identifier.citation | New Journal of Chemistry, 42(2), pp. 1133-1140 | en_US |
dc.identifier.other | https://doi.org/10.1039/C7NJ03964F | - |
dc.identifier.uri | https://pubs.rsc.org/en/content/articlelanding/2018/nj/c7nj03964f#!divAbstract | - |
dc.identifier.uri | http://hdl.handle.net/123456789/2312 | - |
dc.description | Only IISERM authors are available in the record. | - |
dc.description.abstract | A simple ratiometric push–pull and ‘aggregation-induced emission enhancement (AIEE)’ active pyrene based compound, 2-(pyren-1-yl)pyridine (L), was synthesized and characterized by 1H NMR, HRMS and SXRD. The synthesized compound was established as a highly selective and sensitive multi-functional sensor that exhibits a ratiometric fluorescent response, detecting picric acid, H+ and Al3+ [observed sensitivity: 56 nM (12.82 ppb) for picric acid; 2.4 nM (0.27 ppb) for trifluroacetic acid; 2.3 nM (0.86 ppb) for Al3+]. Both L and LH+ have shown emission tuning ability on varying their concentration in solution. Computational calculations (DFT and TD-DFT) have been correlated with the experimental spectroscopic properties. | en_US |
dc.language.iso | en | en_US |
dc.publisher | Royal Society of Chemistry | en_US |
dc.subject | Active pyrene derivative | en_US |
dc.subject | Fluorescent sensor | en_US |
dc.subject | Computational calculations | en_US |
dc.subject | Pyrene derivative | en_US |
dc.title | Simple ratiometric push–pull with an ‘aggregation induced enhanced emission’ active pyrene derivative: a multifunctional and highly sensitive fluorescent sensor | en_US |
dc.type | Article | en_US |
Appears in Collections: | Research Articles |
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