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Highly selective red-emitting H< sub> 2 S fluorescent probe with a large Stokes shift
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Update time: 2014-10-23
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The O-2,4-dinitrobenzensulfonate of 1,3-bis(bispyridin-2ylimino)isoindolin-4-ol has been developed as a novel red-emitting fluorescent probe for the detection of H2S. The dinitrobenzenesulfonate moiety in the probe both prohibits the excited state intramolecular proton transfer process and produces a photo-induced electron transfer process, which renders the probe non-fluorescent in the absence of the analyte. In the presence of H2S a specific H2S-mediated cleavage reaction converts the probe into 1,3-bis(bispyridin-2-ylimino)isoindolin-4-ol which exhibits a strong red fluorescence with a large Stokes shift (218 nm) via an excited state intramolecular proton transfer process upon excitation. It's noteworthy that this new probe shows good selectivity and sensitivity to H2S over glutathione, cysteine and homocysteine. Moreover successful detection and imaging of intracellular H2S in living cells was achieved. To our knowledge this is the first application of this type of fluorescent probe for intracellular H2S detection.
Dyes and Pigments, 2014
Confocal fluorescence contrast images of living A594 cells incubated with 5.0 μBPI-DNBS for 30 min at 37 °C (top row) and further treated with 200.0 μM NaHS for 30 min at 37 °C (bottom row). (a, d) Fluorescence images; (b, e) bright field images; (c, f) fluorescence and bright field overlay images. Scale bar = 10 μm.
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