When crown ethers finally click: Novel, click-assembled, fluorescent enantiopure pyridino-crown ether-based chemosensors - And an: N -2-aryl-1,2,3-triazole containing one

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Abstract

Three novel, click-assembled fluorescent pyridino-18-crown-6 ethers have been synthesized for enantiomeric sensing. We also prepared new azide- and ethynyl-substituted pyridino-18-crown-6 ethers as their precursors, which open the way for further interesting applications using click chemistry. An optically active pyridino-18-crown-6 ether containing an N-2-aryl-1,2,3-triazole type fluorophore unit was also synthesized via post-triazole arylation. These four fluorescent sensor molecules were studied in terms of their optical properties as well as their enantiomeric recognition abilities toward the hydrogen perchlorate salts of 1-phenylethylamine, 1-(1-naphthyl)ethylamine, phenylglycine methyl ester and phenylalanine methyl ester in acetonitrile. This journal is

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Szemenyei, B., Malmosi, M., Pál, D., Baranyai, P., Drahos, L., Móczár, I., & Huszthy, P. (2021). When crown ethers finally click: Novel, click-assembled, fluorescent enantiopure pyridino-crown ether-based chemosensors - And an: N -2-aryl-1,2,3-triazole containing one. New Journal of Chemistry, 45(48), 22639–22649. https://doi.org/10.1039/d1nj04173h

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