Unsymmetrical Schiff base (ON) ligand on complexation with some transition metal ions: Synthesis, spectral characterization, antibacterial, fluorescence and thermal studies

Maha Rabea Abu-Serea; Omyma A.M. Ali; Samir M. El-Medani;

Abstract


A series of eight metal Schiff base complexes were synthesized by the thermal reaction of Cu(II), Ni(II),
Fe(III), Co(II), Zn(II), Hg(II), La(III) or Sm(III) with a Schiff base ‘‘L’’ produced by the condensation of furfuraldehyde
and 1,2-diaminobenzene. These compounds were characterized by elemental analysis,
UV–Vis, FT-IR, molar conductance, mass spectrometry, thermal and fluorescence studies. The studies suggested
the coordination of the ligand L to metal through azomethine imine nitrogen and furan oxygen
atoms of Schiff base moiety. Thermogravimetric (TG/DTG) analyses data were studied and indicated high
stability for all complexes and suggested the presence of lattice and/or coordinated water molecules in
the complexes. Coats–Redfern method has been used to calculate the kinetic and thermodynamic parameters
of the metal complexes. The spectral and thermal analysis reveal that all complexes have octahedral
geometry except Cu(II) and Ni(II) complexes which can attain a square planner arrangements. The ligand
and its complexes exhibited intraligand (p–p⁄) fluorescence and can potentially serve as photoactive
materials. Both the ligand and its complexes have been screened for antibacterial activities.


Other data

Title Unsymmetrical Schiff base (ON) ligand on complexation with some transition metal ions: Synthesis, spectral characterization, antibacterial, fluorescence and thermal studies
Authors Maha Rabea Abu-Serea ; Omyma A.M. Ali ; Samir M. El-Medani 
Keywords Complexes;Spectral;Fluorescence;1,2-Diaminobenzene;Antibacterial activities
Issue Date 2015
Publisher Elsevier
Source Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy 136 (2015) 651–660
Journal Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy 
Volume 136
Start page 651
End page 660
DOI 10.1016/j.saa.2014.09.079

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