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• W1966741881 abstract "The Sharpless–Meldal reaction was employed to generate triazole-substituted, alkynyl, azido and triazolyl-benzoxadiazole as well as nitro-benzoxadiazole fluorophores. Linkage of the triazole to the benzoxadiazole ring at C4 gave chromophores which were fluorogenic, while attachment through N1 resulted in quenching. The 4-azido-7-nitrobenzoxadiazole underwent a 470–fold decrease in quantum yield upon conversion to the triazole. While, 5-ethynyl-benzoxadiazole exhibited a 48–fold enhancement of quantum yield upon formation of triazole. The modulating effects of solvent polarity, conjugation, and attachment point of the fluorochrome to the triazole were examined." @default.
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• W1966741881 date "2011-01-01" @default.
• W1966741881 modified "2023-10-17" @default.
• W1966741881 title "Identification of fluorogenic and quenched benzoxadiazole reactive chromophores" @default.
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• W1966741881 doi "https://doi.org/10.1016/j.dyepig.2010.05.007" @default.
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