Please use this identifier to cite or link to this item: http://hdl.handle.net/123456789/2312
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dc.contributor.authorYadav, H.R.-
dc.contributor.authorChoudhury, A.R.-
dc.date.accessioned2020-11-27T05:45:37Z-
dc.date.available2020-11-27T05:45:37Z-
dc.date.issued2018-
dc.identifier.citationNew Journal of Chemistry, 42(2), pp. 1133-1140en_US
dc.identifier.otherhttps://doi.org/10.1039/C7NJ03964F-
dc.identifier.urihttps://pubs.rsc.org/en/content/articlelanding/2018/nj/c7nj03964f#!divAbstract-
dc.identifier.urihttp://hdl.handle.net/123456789/2312-
dc.descriptionOnly IISERM authors are available in the record.-
dc.description.abstractA 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.isoenen_US
dc.publisherRoyal Society of Chemistryen_US
dc.subjectActive pyrene derivativeen_US
dc.subjectFluorescent sensoren_US
dc.subjectComputational calculationsen_US
dc.subjectPyrene derivativeen_US
dc.titleSimple ratiometric push–pull with an ‘aggregation induced enhanced emission’ active pyrene derivative: a multifunctional and highly sensitive fluorescent sensoren_US
dc.typeArticleen_US
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