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| Content Provider | Springer Nature Link |
|---|---|
| Author | Panchenko, P. A. Fedorov, Yu. V. Fedorova, O. A. Perevalov, V. P. Jonusauskas, G. |
| Copyright Year | 2009 |
| Abstract | A method for the synthesis of N-aryl-substituted 4-amino- and 4-acetylaminonaphthalimide derivatives with mono- and dialkoxy groups or a 15-crown-5 moiety in the N-aryl substituent is described. The introduction of electron-donating alkoxy groups into the benzene ring of the N-aryl fragment results in fluorescence quenching of the naphthalimide chromophore, which is most pronounced in the spectra of N-acetyl derivatives. The photophysical properties of the synthesized 4-amino- and 4-acetylaminonaphthalimides depend on the solvent polarity and its specific solvating ability due to H-bonding. The crown-containing compounds are promising fluorescent chemosensors for metal cations. |
| Starting Page | 1233 |
| Ending Page | 1240 |
| Page Count | 8 |
| File Format | |
| ISSN | 10665285 |
| Journal | Russian Chemical Bulletin |
| Volume Number | 58 |
| Issue Number | 6 |
| e-ISSN | 15739171 |
| Language | English |
| Publisher | Springer US |
| Publisher Date | 2010-04-27 |
| Publisher Place | Boston |
| Access Restriction | One Nation One Subscription (ONOS) |
| Subject Keyword | naphthalimide 15-crown-5 fluorescence hydrogen bond UV-Vis absorption spectra fluorescent sensors 4-nitronaphthalic anhydride photoinduced charge transfer Inorganic Chemistry Organic Chemistry Chemistry/Food Science |
| Content Type | Text |
| Resource Type | Article |
| Subject | Chemistry |
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