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A Reversible Dual Mode Chemodosimeter for the Detection of Cyanide Ions in Natural Sources

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dc.contributor.author Shankar, B H
dc.contributor.author Jayaram, D T
dc.contributor.author Ramaiah, D
dc.date.accessioned 2016-10-27T06:32:52Z
dc.date.available 2016-10-27T06:32:52Z
dc.date.issued 2014-06
dc.identifier.citation Chemistry - An Asian Journal, 9(6):1636-1642 en_US
dc.identifier.uri http://hdl.handle.net/123456789/2484
dc.description.abstract Herein, we report the synthesis of two indolium probes 1 and 2 based on anthracene and pyrene derivatives and their interactions with various anions. Of these probes, the pyrene conjugate 2 acts as a dual colorimetric and fluorescent chemodosimeter for the selective and sensitive detection of cyanide ions. The detection limit of probe 2 for CN(-) ions was found to be 10 ppb (30 nM). The nature of interaction has been thoroughly studied through various techniques such as (1)H NMR and IR spectroscopy, HRMS, and isothermal calorimetric (ITC) studies. These studies confirm that probe 2 forms a 1,2-adduct in the presence of CN(-) ions. Kinetic studies using probe 2 showed the completion of the reaction within 15 s with a rate constant of k' = 0.522±0.063 s(-1). This probe can be coated on a solid surface (dipstick) and a polymer matrix for the on-site analysis and quantification of endogenous cyanide ions in natural sources such as Indian almonds. en_US
dc.language.iso en en_US
dc.publisher Wiley Online Library en_US
dc.subject Indian almonds en_US
dc.subject cyanides en_US
dc.subject dipstick en_US
dc.subject fluorescent probes en_US
dc.subject nucleophilic addition en_US
dc.title A Reversible Dual Mode Chemodosimeter for the Detection of Cyanide Ions in Natural Sources en_US
dc.type Article en_US


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