2001
DOI: 10.1023/a:1007128325639
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Cited by 126 publications
(30 citation statements)
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“…The co-ordination site and binding properties of the ligand are discussed on the basis of spectroscopic analysis. The IR spectra of the ligand and complex were recorded in the 4000-400 cm À1 region and are not similar [24]. The comparison of both spectra reveals the important spectral changes, notably; the characteristic band of carbonyl group t(C@O) in the morin appears at 1662 cm À1 , while in the complex it appears at 1650 cm À1 .…”
Section: Vibrational Spectramentioning
confidence: 97%
“…The co-ordination site and binding properties of the ligand are discussed on the basis of spectroscopic analysis. The IR spectra of the ligand and complex were recorded in the 4000-400 cm À1 region and are not similar [24]. The comparison of both spectra reveals the important spectral changes, notably; the characteristic band of carbonyl group t(C@O) in the morin appears at 1662 cm À1 , while in the complex it appears at 1650 cm À1 .…”
Section: Vibrational Spectramentioning
confidence: 97%
“…Furthermore, the stretching vibration of the amino group in free ABZ observed at 3220 cm -1 is shifted to a lower wave number and . The bands at 3410-3440 cm -1 in the spectra of the complexes are assigned to íOH of the crystalline water molecules 24,25 . Metal-oxygen and metal-nitrogen bonding are manifested by the appearance of bands in the 520-536 cm -1 and 410-440 cm -1 regions respectively 26 .…”
Section: Resultsmentioning
confidence: 99%
“…There are only two absorption bands observed in the spectrum of L1 and L2 in methanol and DMF solutions ( Figures 2 and 3) [16,[27][28][29]. Two peaks at 412 (I) and 238 nm(II) in methanol, 375(I) and 262 nm (II) in DMF; at 403(I) and 236(II) in methanol, at 411(I) and 244 nm(II) in DMF are observed in the spectrum of free L1 and L2, respectively [19][20][21][22]. The observed absorption band at higher wavelength (lower frequency) is assigned to the p-p and n-p transitions, and a second band observed at lower wavelength (higher frequency) is due to Main Group Chemistry 135 the p-p and n-s transitions, that correspond to ring A (quinolic system) and ring B (catechol system), respectively [28,29].…”
Section: Uv-vis Spectramentioning
confidence: 94%
“…Some flavonoids possess strong antioxidant activity through their ability to scavenge free radicals and chelate metal ions [15][16][17][18][19][20]. The chelating capacities of flavonoids with metal ions such as transition and non-transition metals have been reported earlier and demonstrated that their coordination complexes were better inhibitors of free radicals than the ligands alone [17][18][19][20]21]. As a result of their potential utility in biomedical science flavonoid coordination chemistry has been extensively studied [15][16][17][18][19][20][21][22][23][24][25].…”
Section: Introductionmentioning
confidence: 99%