2010
DOI: 10.4314/bajopas.v2i1.58524
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Synthesis and characterization of iron (ii) and nickel (ii) schiff base complexes

Abstract: The complexes of iron (II) and nickel (II) with schiff base derived from benzoin and 2-amino benzoic acid have been prepared. Solubility, melting point, decomposition temperature, conductance measurement, infrared (IR) and UV-Visible spectrophotometric studies were used in characterizing the compounds. The melting point of the schiff base determined is 120 o C. The decomposition temperatures of iron (II) and nickel (II) complexes are 152 o C and 155 o C, while the molar conductance values are 11.2 and 10.7 ohm… Show more

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Cited by 8 publications
(7 citation statements)
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“…Moreover the new band in the far infrared spectra of the complexes in the range 584-615 cm -1 is assigned to the mM-N. Deprotonation of all hydroxyl functions is confirmed by the lack of Oxime N-O-H and shift of mN-O to higher wave number to about 1059-1063 cm -1 but appeared in free ligand at 1030 cm -1 , indicating the participation with the metal ion as -O -. The broadening bands observed in the spectra of complexes in the range 3377-3488 cm -1 considerable support the presence of water molecules in the complexes [24,32,33]. The weak bands appeared in the far IR spectra between 615-660 cm -1 were attributed to mM-O.…”
Section: Ir Spectramentioning
confidence: 70%
“…Moreover the new band in the far infrared spectra of the complexes in the range 584-615 cm -1 is assigned to the mM-N. Deprotonation of all hydroxyl functions is confirmed by the lack of Oxime N-O-H and shift of mN-O to higher wave number to about 1059-1063 cm -1 but appeared in free ligand at 1030 cm -1 , indicating the participation with the metal ion as -O -. The broadening bands observed in the spectra of complexes in the range 3377-3488 cm -1 considerable support the presence of water molecules in the complexes [24,32,33]. The weak bands appeared in the far IR spectra between 615-660 cm -1 were attributed to mM-O.…”
Section: Ir Spectramentioning
confidence: 70%
“…, and C=N at 1598 cm , showing that electrons on the nitrogen of the azomethine group were involved in the formation of the coordinate bond with the central metal atom [17]. The appearance of additional bands at 508-518 cm -1 and 530-550 cm -1 revealed the nature of the metal-ligand relationship, which illustrates (M-N) and (M-O) bonding in the ligand.…”
Section: Spectral Characterizationmentioning
confidence: 95%
“…Further the band at 1728cm -1 , υ (C=O) ketonic carbonyl and a band at 1628cm -1 due to υ (C=N) azomethine group shifted towards lower values in metal chelates indicating that carbonyl oxygen and azomethine group of isatin residue is the coordinating sites 20,21 . Appearance of a new bands at 3390cm -1 in Ti(IV) 22 , 3355cm -1 in Zr(IV) 23 and 3350cm -1 in Cd(II) complexes 24 suggested presence of coordinated water molecules. The new bands in spectra of Ti(IV), Zr(IV), Cd(II) and Hg(II) metal complexes at 491-635 cm -1 due to υ (M-N) [25][26][27][28] .…”
Section: Infrared Spectramentioning
confidence: 98%