A novel 1,8-naphthalimide probe for selective determination of Hg2+ in a wide pH window
creativework.keywords | 1,8-Naphthalimide, Aggregation caused quenching, Fluorescent probe, Hg2+ | |
creativework.publisher | University of Chemical Technology and Metallurgyjournal@uctm.edu | en |
dc.contributor.author | Krasteva P. | |
dc.contributor.author | Dimitrova M. | |
dc.contributor.author | Georgiev N. | |
dc.contributor.author | Bojinov V. | |
dc.date.accessioned | 2024-07-16T11:16:48Z | |
dc.date.accessioned | 2024-07-16T11:18:50Z | |
dc.date.available | 2024-07-16T11:16:48Z | |
dc.date.available | 2024-07-16T11:18:50Z | |
dc.date.issued | 2018-01-01 | |
dc.description.abstract | This paper reports the synthesis and photophysical investigation of a novel 1,8-naphthalimide fluorophore containing 2-amino-1,3,4-thiadiazole fragment at C-4 position. Absorption and fluorescence characteristics of the dye as a function of pH were investigated in water/ethanol (1:1, v/v) solution. It was found that the synthesized 1,8-naphthalimide did not show significant changes in the emission properties in a wide pH range. Furthermore the ability of the synthesized compound to detect cations was evaluated by the changes in its fluorescence intensity in the presence of metal ions (Co2+, Cu2+, Fe3+, Ni2+, Pb2+, Cd2+, Zn2+ and Hg2+). Only Hg2+, among the tested metal ions, was efficiently detected due to the aggregation caused quenching process. The results obtained indicate the potential of the novel compound acting as a fluorescent ``onoff`` switch for selective determination of Hg2+ in a wide pH window. | |
dc.identifier.issn | 1314-7978 | |
dc.identifier.issn | 1314-7471 | |
dc.identifier.scopus | SCOPUS_ID:85042076735 | en |
dc.identifier.uri | https://rlib.uctm.edu/handle/123456789/1196 | |
dc.language.iso | en | |
dc.source.uri | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85042076735&origin=inward | |
dc.title | A novel 1,8-naphthalimide probe for selective determination of Hg2+ in a wide pH window | |
dc.type | Article | |
oaire.citation.issue | 2 | |
oaire.citation.volume | 53 |