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Luminescence ; 29(8): 1113-22, 2014 Dec.
Article in English | MEDLINE | ID: mdl-24846775

ABSTRACT

Eight novel 1,2,4-triazolo[3,4-b]-1,3,4-thiadiazol derivatives have been designed and synthesized, and their corresponding Tb(3+) complexes were also prepared successfully. The fluorescence properties and fluorescence quantum yields of the target complexes were investigated, the results showed that the ligands were an efficient sensitizer for Tb(3+) luminescence, and the target complexes exhibited characteristic fluorescence emissions of Tb(3+) ion. The fluorescence intensity of the complex substituted by chlorine was stronger than that of other complexes. The substituents' nature has a great effect upon the electrochemical properties of the target complexes. The results showed that the introduction of the electron-withdrawing groups tended to decrease the oxidation potential and highest occupied molecular orbital energy levels of the target Tb(3+) complexes; however, introduction of the electron-donating groups can increase the corresponding complexes' oxidation potential and highest occupied molecular orbital energy levels.


Subject(s)
Terbium/chemistry , Thiadiazoles/chemistry , Chemistry Techniques, Synthetic , Chlorine/chemistry , Electrochemical Techniques , Fluorescence , Molecular Structure , Solubility , Spectrometry, Fluorescence , Spectrophotometry, Infrared , Spectrophotometry, Ultraviolet , Spectroscopy, Fourier Transform Infrared , Structure-Activity Relationship , Thiadiazoles/chemical synthesis
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