| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5274706 | Tetrahedron Letters | 2012 | 6 Pages |
Abstract
The preparation of N,Nâ²-diarylalkanediamides from the respective aliphatic dicarboxylic acids and 4-nitroaniline via microwave-prompted reactions is presented. The most positive effect of microwave irradiation was observed for N,Nâ²-bis(4-nitrophenyl)butanediamide. Anion binding studies on the obtained diamides were carried out in DMSO and acetonitrile using UV-vis and 1H NMR spectroscopy. A mechanism for selective fluoride recognition by N,Nâ²-bis(4-nitrophenyl)butanediamide in DMSO is proposed.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Ewa Wagner-Wysiecka, Natalia Åukasik,