Enhancement of the fluorescence intensity of Se-2,3-diaminonaphthalene complex in aqueous solution by adding organic solvents
✍ Scribed by E.M.Rodríguez Rodríguez; M.Sanz Alaejos; C.Díaz Romero
- Publisher
- Elsevier Science
- Year
- 1996
- Tongue
- English
- Weight
- 459 KB
- Volume
- 334
- Category
- Article
- ISSN
- 0003-2670
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✦ Synopsis
Fluorescence of the Se-2,3_diaminonaphthalene (DAN) complex has been studied in aqueous solutions with several organic solvents. With all organic solvents, the wavelength of the emission maxima in water was shifted to shorter wavelengths. However, the wavelength of the excitation maxima did not change. Fluorescence intensity (Z,) of the Se-DAN complex observed with most organic media, increased with respect to the Z, observed in water. However, the precision was poorer using the organic solvents than the precision found in water. Tetrahydrofuran (90%) and 1,4-dioxane (90%) exhibit the highest increases of Z, Higher enhancements of Z, of the Se-DAN complex were observed when the concentration of organic solvent increased. So, the equations In Z, = a + b. (% organic solvent)2i3 and ~/IF = a + b. (% organic solvent)"* could be established. Maximum IF of the Se-DAN complex in the studied organic media was obtained at a pH between 2.5 and 3.5. Tetrahydrofuran and acetonitrile showed the highest stability in the presence and absence of sunlight. Tetrahydrofuran (90%) and acetonitrile (60%) presented the best detection limits 1.96 and 3.00 pg Se l-', respectively, showing a 23-and 15-fold improvement of the detection limit in aqueous medium. Acetonitrile (60%) was satisfactorily compared with hydride generation-atomic absorption spectrometry.
📜 SIMILAR VOLUMES
A series of lower rim 1,3-di-derivatives possessing Schiff's base cores were synthesized using triazole unit as linker moiety by further introducing butyl (L 2 ), one -CH 2 OH (L 3 ) and two -CH 2 OH (L 4 )-containing moieties, respectively, in order to bring additional support for ion binding. Base