Issue 7, 2014

Assembly of indole fluorophore in situ for hydrogen sulfide signaling through substrate triggered intramolecular reduction–cyclization cascade: a sensitive and selective probe in aqueous solution

Abstract

A novel probe containing the azide–coumarin–aldehyde triad (S1) for hydrogen sulfide (H2S) was developed. The fluorophore for signaling is assembled in situ through a H2S triggered intramolecular reduction–cyclization cascade, and has a concomitant 10-fold enhancement of the fluorescent intensity at 520 nm. Fluorescence imaging of H2S in living cells proved its potential for biological application.

Graphical abstract: Assembly of indole fluorophore in situ for hydrogen sulfide signaling through substrate triggered intramolecular reduction–cyclization cascade: a sensitive and selective probe in aqueous solution

Supplementary files

Article information

Article type
Letter
Submitted
23 Nov 2013
Accepted
18 Mar 2014
First published
19 Mar 2014

New J. Chem., 2014,38, 2770-2773

Author version available

Assembly of indole fluorophore in situ for hydrogen sulfide signaling through substrate triggered intramolecular reduction–cyclization cascade: a sensitive and selective probe in aqueous solution

J. Zhou, Y. Luo, Q. Li, J. Shen, R. Wang, Y. Xu and X. Qian, New J. Chem., 2014, 38, 2770 DOI: 10.1039/C3NJ01465G

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