“…Hydrogen sulfide has sparked vast creativity in the design of reaction-based triggers for this reactive analyte, and these can be generally categorized into reduction-based triggers, electrophilic triggers, copper-based triggers, and a few other interesting developments, including triggers incorporating molecular recognition (Figures – ). Reduction-based triggers include azides, − sulfonyl azides, , nitro groups, − nitroso groups, and quinones . A wide variety of electrophilic triggers that operate via hydrogen sulfide’s nucleophilicity have been developed including aldehyde-assisted ester cleavage, aldehyde-assisted conjugate addition, aldehyde-assisted dinitrophenyl cleavage, nucleophilic aromatic substitution, , nucleophilic addition to an imine, , nitrobenzoxadiazole with amine ,− or alcohol , leaving groups, vinyl chloride substitution alone or followed by cyclization, an aryl cyanate, disulfide-assisted ester cleavage, − diselenide-assisted ester cleavage,…”