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• W2018892186 abstract "Several N-alkyl and N-phenyl derivatives of 6-amino- () and 6,6'-diamino-2,2':6',2''-terpyridine () were synthesized, and their fluorescence properties were studied. A successive red-shift was observed as the number of the N-substituted groups increased. It was also shown that the susceptivity of the fluorophores to a solvent varied considerably according to the mode of the N-substitution. While the monoamino-tpys (tpy: 2,2':6',2''-terpyridine) suffered almost complete quenching of their fluorescence in ethanol, the fully N-alkylated diamino-tpys and retained their fluorescence. The results show that N-substitution is a useful way to tune both the radiation energy and solvent susceptivity of the fluorescence of the amino-tpys." @default.
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• W2018892186 date "2007-01-01" @default.
• W2018892186 modified "2023-10-14" @default.
• W2018892186 title "Tuning of fluorescence properties of aminoterpyridine fluorophores by N-substitution" @default.
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• W2018892186 doi "https://doi.org/10.1039/b707662b" @default.
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