Synthesis, characterization and solid state conductivity of nano-size ionic Schiff base polymers of Cu2+, Zn2+ and VO2+ containing viologen moieties

2019 ◽  
Vol 43 (42) ◽  
pp. 16468-16477
Author(s):  
Zohreh S. Ghavami ◽  
Gholamhossein Grivani

The new nano size ionic metallo-Schiff base polymers (IMSPs) were synthesized by reaction of Schiff base ligand of L and VO (acac)2, ZnCl2 and CuCl2. The solid state conductivity measurements candidate them as new metallo-organic semiconductors.

2018 ◽  
Vol 71 (6) ◽  
pp. 874-889 ◽  
Author(s):  
Sebastián Martínez ◽  
Fernando Igoa ◽  
Ignacio Carrera ◽  
Gustavo Seoane ◽  
Nicolás Veiga ◽  
...  

2021 ◽  
Vol 2063 (1) ◽  
pp. 012004
Author(s):  
Atared F. Hassan ◽  
Hiba H. Sabah ◽  
Afaq A. Turki

Abstract A new series of Co(II), Fe(II), Cu(II) and Ni(II) complexes of Bis–(4-benzylidenamino-phenyl)-methane (L) have been prepared and characterized. The complexes conform to general formula [CoL(H2O)3] Cl2, [FeL(H2O)5]SO4.2H2O, [CuL(H2O)5] NO3 and [NiL(H2O)3Cl2], Infra red spectra and elemental analysis reveal uni-dentate coordination of Schiff base to metal ions. Molar conductivity measurements show that complexes (I, III) behave as 2:1 electrolyte while complex (II) behave as 1:1 electrolyte. The thermal studies for complexes shows that the complexes are thermal stable.


2019 ◽  
Vol 43 (35) ◽  
pp. 13916-13928 ◽  
Author(s):  
Lukáš Pogány ◽  
Barbora Brachňaková ◽  
Petra Masárová ◽  
Ján Moncol ◽  
Ján Pavlik ◽  
...  

A series of novel iron(iii)-Schiff base complexes have been prepared and structurally characterised. Their stereochemical, magnetic and redox properties were correlated with the molecular design of the corresponding N3O2-pentadentate Schiff base ligand.


2006 ◽  
Vol 62 (5) ◽  
pp. m948-m949 ◽  
Author(s):  
Yu-Ye Yu

The title compound, [Ni(C18H18N2O4)]·CHCl3, has been synthesized by the solid-state reaction of Ni(OAc)2·4H2O and the Schiff base ligand N,N′-ethylene-bis(3-methoxysalicylaldehyde) [abbreviated as H2(3-MeO-salen)]. The Ni atom adopts a slightly deformed square-planar coordination geometry in which the 3-MeO-salen ligand acts as a cis-N2O2 donor.


2021 ◽  
Author(s):  
Yasmin mamdoh hussien Ahmed ◽  
Gehad G. Mohamed

Abstract A new tetradentate Schiff base ligand was prepared from condensation of 4,6-dihydroxy-1,3-phenylenediethanone with ethane-1,2-diylbis(oxy)diethanamine. The ligand forms complexes in good yield. The Schiff base and its complexes were characterized by analytical (CHN elemental analyses, solubility, melting point, conductivity) measurements, spectral (IR, UV-vis, 1H NMR and MS) and magnetic measurements. The elemental analyses, Uv-vis spectra, and room temperature magnetic moment data and theoretically through density function theory were used as characterizing techniques in supporting of further interpretation of the complexes structures. The results of elemental analyses, EI-mass and conductivity measurements confirmed the stoichiometry of the ligand and its complexes while the characteristic absorption bands and resonance peaks in IR and NMR spectra confirmed the formation of the ligand frameworks around the metal ions. The octahedral environment for complexes derived from Schiff base ligand have been confirmed on the basis of results of electronic and diffused reflectance spectral studies and magnetic moment measurements. Detailed studies of the thermal properties of the Schiff base ligand and complexes were investigated by thermogravimetric technique. Moreover, the molecular docking into (PDB: 6NE0) was the DNA binding and supports the experimental finding and 6IY0 Crystal structure of conserved hypothetical protein SAV0927 from Staphylococcus aureus subsp. aureus Mu50. The synthesized ligand and its complexes were tested for in vitro antimicrobial activity against Candida albicans, Bacillus subtilis, Aspergillus flavus, Escherichia coli, Pseudomonas aeruginosa and Staphylococcus aureus by using agar-well diffusion method.


2011 ◽  
Vol 2011 ◽  
pp. 1-8 ◽  
Author(s):  
C. Anitha ◽  
S. Sumathi ◽  
P. Tharmaraj ◽  
C. D. Sheela

A series of metal(II) complexes ML where M = VO(II), Co(II), Ni(II), Cu(II), and Zn(II) have been synthesized from azo Schiff base ligand (N′E)-N′-(5-((4-chlorophenyl)diazenyl)-2-hydroxybenzylidene)-2-hydroxybenzohydrazide and characterized on the basis of elemental analyses, electronic, IR, and 1H NMR spectra, magnetic susceptibility and also by aid of scanning electron microscopy (SEM), X-ray powder diffraction, fluorescence spectral studies, and molar conductivity measurements. Conductivity measurements reveal that the complexes are nonelectrolytes. Spectroscopy and other analytical studies reveal distorted square planar geometry for copper, square-pyramidal geometry for oxovanadium, and tetrahedral geometry for other complexes. Redox behavior of the copper(II) complex has been studied with cyclic voltammetry, and the biological activities of the ligand and metal complexes have been studied against several microorganisms by the well diffusion method. All synthesized compounds can serve as potential photoactive materials as indicated from their characteristic fluorescence properties. The second harmonic generation (SHG) efficiency of the ligand was measured and found to be higher than that of urea and KDP. The SEM image of the copper(II) complex implies that the size of the particles is 50 nm.


2018 ◽  
Vol 9 (1) ◽  
pp. 92-100 ◽  
Author(s):  
Niaz Monadi ◽  
Samira Saeednia ◽  
Parvaneh Iranmanesh ◽  
Mehdi H. Ardakani ◽  
Samira Sinaei

Introduction: In this study the synthesis and characterization of copper oxide nanoparticles via solid state thermal decomposition of a recently synthesized aqua nitrato copper(II) complex with a tridentate Schiff-base ligand (1) as a new precursor are reported. Materials & Methods: The copper complexes were obtained by sonochemical and solvothermal process and characterized by Scanning Electron Microscopy (SEM), X-ray powder Diffraction (XRD) and FT-IR spectroscopy. The thermal stability of compound (1) was studied by Thermogravimetric Analysis (TGA). The amount of initial reagents and the role of reaction time on size and morphology of nanostructure compound (1) were studied. CuO nanoparticles were simply synthesized at 500 oC under air atmosphere. Results & Conclusion: The diameter of CuO nanoparticles was estimated to be about 200 and 30 nm from copper complex precursor obtained by sonochemical and solvothermal methods respectively.


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