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- W2766082563 abstract "A newly synthesized and characterized naphthalimide derivative (L1) acts as a highly sensitive chemosensor for aqueous sulfide ions in water/DMSO (3:1, v/v) medium as L1 offers distinctive reactive properties toward aqueous sulfide ions to be converted to L1A of potential turn-on fluorescent properties over other competitive anions. Gradual addition of aqueous sulfide ions led to the formation of in situ L1A compound which showed a single point fluorescence enhancement based on intramolecular charge transfer (ICT). To establish this new interesting pathway in favor of ICT for sensing sulfide ions, the detailed spectroscopic studies of other three similar type new 1,8-naphthalimide based organic probes (L2, L3 and L4) duly structurally characterized including theoretical (DFT) studies have been carried out systematically. The probe (L1) detects aqueous sulfide ions as low as 2.4 μM in at biological pH within a very short responsive time (15-20 s) and this non-cytotoxic the probe, L1 is also useful in acquiring the fluorescent image of the distribution of sulfide ions in living cells using fluorescence microscope." @default.
- W2766082563 created "2017-11-10" @default.
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- W2766082563 date "2017-10-31" @default.
- W2766082563 modified "2023-09-27" @default.
- W2766082563 title "Naphthalimide-Based Turn-On Fluorosensor for Aqueous Sulfide Ions for Staining in Living Cells" @default.
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- W2766082563 doi "https://doi.org/10.1002/slct.201701351" @default.
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