Abstract
Many fluorophores, and all bright light-emitting
substrates for firefly luciferase, contain hydroxyl or amine electron donors.
Here we show that sulfonamides can serve as replacements for these canonical
groups. Unlike “caged” carboxamides, sulfonamide analogues enable
bioluminescence, and sulfonamidyl luciferins, coumarins, rhodols, and
rhodamines are fluorescent in water. Sulfonamide donors thus have previously unappreciated
potential to expand the functional repertoire of luminescent molecules.
Supplementary materials
Title
Sulfonamide manuscript for uploading
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Sulfonamide Manuscript SI with NMR
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Sulfonamide Manuscript TOC
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