A novel
fluorescence probe, HBTSeSe, was designed and synthesized
for the detection of H
2
S with a double-switch mechanism
of a broken diselenide bond followed by thiolysis of ether. Then,
2-(2′-hydroxyphenyl)benzothiazole (HBT) was released as fluorophore,
which has large Stokes shift based on the excited state intramolecular
proton transfer process. The probe responded selectively and rapidly
to H
2
S, with the fluorescence increased by 47-fold immediately
after the addition of H
2
S. HBTSeSe was able to detect H
2
S in the cytoplasm, specifically in cell imaging experiments.
The results also showed that H
2
S was produced in the immune
response of RAW264.7 cells activated by phorbol-12-myristate-13-acetate.