Photo- and ionochromic indolylmaleimides containing naphthalimide linkers
Newly synthesized indolyl(thienyl)maleimides containing naphthalimide linkers were found to exhibit weak fluorescence due to PET effect. Irradiation at 436 nm wavelength led to the formation of their cyclic isomers. The obtained compounds showed the properties of chromogenic and fluorogenic chemosen...
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Published in | Chemistry of heterocyclic compounds (New York, N.Y. 1965) Vol. 54; no. 1; p. 32 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
Springer
01.01.2018
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Abstract | Newly synthesized indolyl(thienyl)maleimides containing naphthalimide linkers were found to exhibit weak fluorescence due to PET effect. Irradiation at 436 nm wavelength led to the formation of their cyclic isomers. The obtained compounds showed the properties of chromogenic and fluorogenic chemosensors for F.sup.- ions. |
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AbstractList | Newly synthesized indolyl(thienyl)maleimides containing naphthalimide linkers were found to exhibit weak fluorescence due to PET effect. Irradiation at 436 nm wavelength led to the formation of their cyclic isomers. The obtained compounds showed the properties of chromogenic and fluorogenic chemosensors for F.sup.- ions. |
Audience | Academic |
Author | Podshibyakin, Vitaly A Bren, Vladimir A Tikhomirova, Karina S Dubonosov, Alexander D Shepelenko, Evgenii N Revinskii, Yurii V |
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DOI | 10.1007/s10593-018-2226-x |
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Title | Photo- and ionochromic indolylmaleimides containing naphthalimide linkers |
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