2012
DOI: 10.1016/j.ica.2012.03.029
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Synthesis, characterization, biological activities, and luminescent properties of lanthanide complexes with N,N′-bis(2-hydroxy-1-naphthylidene)-1,6-hexadiimine

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Cited by 40 publications
(27 citation statements)
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“…The ligands possessed multiple aromatic rings, triazole and thiadiazole rings with a rigid planar skeleton structure that has a strong antenna effect. In order to obtain luminescence, the lowest triplet state energy of the ligand, must be close or lie above the resonance energy of the Eu(III) ions [23]. Among the eight complexes, it is clearly observed that the complexes substituted by the electron-withdrawing group have stronger luminescence intensities, this may be ascribed to triplet level of the ligands be lowered by the electron-withdrawing groups, thus the triplet state energy level of the ligands approaching to the resonance level of Eu(III), which makes the energy transition from ligands to Eu(III) more easily.…”
Section: Complexesmentioning
confidence: 99%
“…The ligands possessed multiple aromatic rings, triazole and thiadiazole rings with a rigid planar skeleton structure that has a strong antenna effect. In order to obtain luminescence, the lowest triplet state energy of the ligand, must be close or lie above the resonance energy of the Eu(III) ions [23]. Among the eight complexes, it is clearly observed that the complexes substituted by the electron-withdrawing group have stronger luminescence intensities, this may be ascribed to triplet level of the ligands be lowered by the electron-withdrawing groups, thus the triplet state energy level of the ligands approaching to the resonance level of Eu(III), which makes the energy transition from ligands to Eu(III) more easily.…”
Section: Complexesmentioning
confidence: 99%
“…The prior studies have focused on preparation and characterization of complexes of europium (III) metal ion with organic reagents [46]. On the other hand, previous studies concerning the antibacterial and antifungal activity of ligand and its metal complexes tested against gram-positive and gram-negative bacteria, yeast, and fungi show that the complexes are more potent antimicrobials than the parent ligand [47][48][49].…”
Section: Introductionmentioning
confidence: 99%
“…This result confirmed that the pyridine N atom is not involved in the coordination. Further evidence for the coordination through both N and O atoms comes from the appearance of two new non‐ligand bands at 430 and 477 cm −1 , which were tentatively assigned to ν(Eu–O) and ν(Eu–N), respectively, Figure (ii) . Moreover, the presence of a broad band extending from 3700 to 3250 cm −1 with two maxima at 3420 and 3265 cm −1 could mean that uncoordinated water molecules are present in the complex, as is evident from the TGA study.…”
Section: Resultsmentioning
confidence: 99%