Publication | Open Access
A highly selective chemodosimeter for fast detection and intracellular imaging of Hg<sup>2+</sup>ions based on a dithiocarbamate–isothiocyanate conversion in aqueous ethanol
33
Citations
60
References
2013
Year
Selective ChemodosimeterEngineeringOrganic ChemistryChemistryNew Naphthalene Diimide-dithiocarbamateAnalytical ChemistryBioimagingCation SensingChemical SensorMolecular ImagingPhotophysical PropertyFluorescence ProbeChemical MeasurementBiochemistryPhotochemistryAtomic Fluorescence SpectroscopyVarious Metal IonsIntracellular ImagingMolecular ModelingSingle-molecule DetectionBiomolecular EngineeringNatural SciencesChemical ProbeDithiocarbamate–isothiocyanate ConversionDrug Analysis
A new naphthalene diimide-dithiocarbamate based fluorescence probe was synthesized and its fluorogenic behavior towards various metal ions was studied. Upon addition of various metal ions, the probe afforded an irreversible change only with Hg(2+) ions in aqueous-ethanol media (4 : 1 v/v) with a fourfold enhancement of the fluorescence (Φ = 0.03 → 0.11) along with a distinct 43 nm blue shift of the emission maxima. The mechanism of the chemodosimetric behavior of the probe has been attributed to a Hg(2+) induced transformation of a weakly fluorescent dithiocarbamate to a highly fluorescent isothiocyanate which has been characterized by a number of spectroscopic techniques and a crystal structure. Intracellular detection of Hg(2+) ions was achieved using the probe.
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