Journal
ORGANIC & BIOMOLECULAR CHEMISTRY
Volume 10, Issue 15, Pages 3104-3109Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/c2ob06980f
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Funding
- National Science Foundation of China [20902021, 21002013]
- Scientific Research Foundation for the Returned Overseas Chinese Scholars (State Education Ministry)
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Here, we report a new Cu2+-selective fluorescent turn-on probe BODIPY-EP, in which the 2-pyridinecarboxylic acid is connected to a 6-hydroxyindole-based BODIPY platform through an ester linkage. The ester bond of BODIPY-EP is selectively hydrolyzed by the reaction with Cu2+ under mild and neutral conditions to generate BODIPY-OH, showing strong characteristic fluorescence of BODIPY-OH. The favorable features of BODIPY-EP towards Cu2+ include fast response, large fluorescence enhancement and high selectivity. We further demonstrated that the membrane-permeable probe reacts with intracellular Cu2+ and exhibits bright fluorescence in living cells.
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