2013
DOI: 10.1016/j.saa.2012.10.058
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Spectroscopic and density functional theory investigation of novel Schiff base complexes

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Cited by 50 publications
(29 citation statements)
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“…The E binding of the complexes are about 4% higher than our previously reported complexes with a similar Schiff base structure namely 1,2‐bis[(2‐(2‐mercaptophenylimino)‐methyl)phenoxy]ethane using the same level of theory that may suggests a possibility of more stable complexes with phenolic Schiff base than thio‐phenolic ones.…”
Section: Discussionmentioning
confidence: 53%
“…The E binding of the complexes are about 4% higher than our previously reported complexes with a similar Schiff base structure namely 1,2‐bis[(2‐(2‐mercaptophenylimino)‐methyl)phenoxy]ethane using the same level of theory that may suggests a possibility of more stable complexes with phenolic Schiff base than thio‐phenolic ones.…”
Section: Discussionmentioning
confidence: 53%
“…On the other hand, the Fe(III) complex has a molar conductance value of 250 Ω −1 mol −1 cm 2 , indicating its ionic nature and it is considered as a 1:3 electrolyte. [29][30][31] 3.3 | FT-IR spectra and mode of bonding…”
Section: Molar Conductance Measurementsmentioning
confidence: 99%
“…[20,[23][24][25][26][27][28][29][30] The absent of the band at 1728 cm -1 in complexes and the shift of the characteristic band of azomethine group to a lower value from 1624 cm -1 to 1578 cm -1 for Cr(III), Fe(III) and Co(II), at 1574 cm -1 for Mn(II), at 1570 cm -1 for Ni(II) indicate that the involvement of C=N group and oxygen of carboxylic group in the interaction with metal ion forming five and six membered rings and the carboxylic group is deprotonated. [31,32] In the case of monodentate carboxylate ligand, the antisymmetric and symmetric COOstretches will be shifted to higher and lower frequencies, respectively, with an average ∆ν>200 cm -1 . [33][34][35] For our complexes the presence of bands with different intensities in the region1628-1620 cm -1 in the IR spectra of the metal ciprofloxacin Schiff base complexes can be assigned to the asymmetric stretching vibration ν as ( C=O) of the ligated carboxylato group and the symmetric vibration occurs in the region 1389-1377 cm -1 with different intensities, [36][37][38][39] with ∆ν>200 cm -1…”
Section: Ir Absorption Spectramentioning
confidence: 99%