Synthesis, crystal structures, spectral studies and reactivity of square planar copper(II) complexes containing Schiff base ligand

2013 ◽  
Vol 66 (4) ◽  
pp. 568-579 ◽  
Author(s):  
Poulami Pattanayak ◽  
Jahar Lal Pratihar ◽  
Debprasad Patra ◽  
Chia-Her Lin ◽  
Paula Brandão ◽  
...  
Keyword(s):  
Schiff Base ◽  
Crystal Structures ◽  
Schiff Base Ligand ◽  
Spectral Studies ◽  
Square Planar

Square Planar Complexes of Cu(II) with an N2O Donor Set of a New Schiff Base Ligand: Synthesis and Structural Aspects

2004 ◽  
Vol 59 (6) ◽  
pp. 655-660 ◽  
Author(s):  
Pritha Talukder ◽  
Amitabha Datta ◽  
Samiran Mitra ◽  
Georgina Rosair
Keyword(s):  
Schiff Base ◽  
Crystal Structures ◽  
Schiff Base Ligand ◽  
Condensation Product ◽  
Planar Geometry ◽  
Square Planar ◽  
Square Planar Complexes ◽  
Tridentate Schiff Base ◽  
Copper Centre ◽  
Structural Aspects

The title compounds, [Cu(C16H23N2O)SCN] (1) and [Cu(C16H23N2O)N3] (2), containing a tridentate Schiff base ligand, which is the 1:1 condensation product of benzoylacetone and 2- diethylaminoethylamine, have been synthesised and their crystal structures determined. The structure of 1 is based on a four coordinate copper centre with square-planar geometry formed by the N2O donor set of the Schiff base and an N atom of the thiocyanate anion. A similar arrangement occurs in 2 with the N2O donor set of the Schiff base and an N atom of the azide anion. The Cu-N and Cu-O distances are 1.924(8), 2.073(8), 1.927(9) and 1.910(6)Å , for 1 and 1.960(4), 2.050(4), 1.935(4) and 1.907(3) for 2, respectively.

Chelates of nickel(II) and copper(II) with tridentate Schiff base formed by the condensation of S-benzyldithiocarbazate with benzoin

1978 ◽  
Vol 56 (15) ◽  
pp. 2000-2002 ◽  
Author(s):  
M. T. H. Tarafder ◽  
M. Akbar Ali
Keyword(s):  
Schiff Base ◽  
Spectral Data ◽  
General Formula ◽  
Schiff Base Ligand ◽  
Nickel Complexes ◽  
Planar Structure ◽  
Spectral Studies ◽  
Square Planar ◽  
Elemental Analyses ◽  
Tridentate Schiff Base

New complexes with the Schiff base ligand derived from S-benzyldithiocarbazate (NH2—NH—CSSCH2C6H5) have been prepared and characterized by elemental analyses, magnetic, conductometric, ir, and electronic spectral studies. The tridentate ONS Schiff base S-benzyl-β-N-(phenyl, phenylhydroxymethyl)methylenedithiocarbazate gave mono-ligand complexes with Ni(II) and Cu(II) having the general formula [MligandX] (M = Ni(II) and Cu(II); X = NO3, Cl, Br, NCS). A proposed square-planar structure for the nickel complexes is supported by magnetic and spectral data. A square-planar structure is also suggested for Cu(II) complexes. The ir results give evidence of the different bondings present in the complexes.

Synthesis, crystal structures and spectral studies of square planar nickel(II) complexes containing an ONS donor Schiff base and triphenylphosphine

Polyhedron ◽  
2009 ◽  
Vol 28 (11) ◽  
pp. 2157-2164 ◽  
Author(s):  
M. Muthu Tamizh ◽  
Kurt Mereiter ◽  
Karl Kirchner ◽  
B. Ramachandra Bhat ◽  
R. Karvembu
Keyword(s):  
Schiff Base ◽  
Crystal Structures ◽  
Spectral Studies ◽  
Square Planar

{1-[2-(Methylamino)ethyliminomethyl]naphthalen-2-olato}thiocyanatocopper(II)

2006 ◽  
Vol 62 (7) ◽  
pp. m1533-m1534 ◽  
Author(s):  
Han-Na Hou
Keyword(s):  
Schiff Base ◽  
Schiff Base Ligand ◽  
Title Compound ◽  
Planar Geometry ◽  
Asymmetric Unit ◽  
Thiocyanate Anion ◽  
Square Planar

The title compound, [Cu(C14H15N2O)(NCS)], is a mononuclear copper(II) complex, with two molecules in the asymmetric unit. The CuII ion is coordinated by one O and two N atoms of a Schiff base ligand, and by one N atom of a thiocyanate anion, forming a square-planar geometry.

Heteronuclear Ni(ii)–Ln(iii) (Ln = La, Pr, Tb, Dy) complexes: synthesis and single-molecule magnet behaviour

2016 ◽  
Vol 45 (8) ◽  
pp. 3616-3626 ◽  
Author(s):  
Apoorva Upadhyay ◽  
Chinmoy Das ◽  
Stuart K. Langley ◽  
Keith S. Murray ◽  
Anant K. Srivastava ◽  
...  
Keyword(s):  
Magnetic Susceptibility ◽  
Schiff Base ◽  
Crystal Structures ◽  
Single Molecule ◽  
Schiff Base Ligand ◽  
Ac Magnetic Susceptibility ◽  
Frequency Dependent ◽  
Single Molecule Magnet

The crystal structures are reported for three heterometallic Ni2Ln and a Ni2Dy2 complex, using the Schiff base ligand 2-methoxy-6-[(E)-phenyliminomethyl] phenol. Detailed dc and ac magnetic susceptibility studies were reported for all the complexes. The complexes 3 and 4 shows frequency dependent out-of-phase susceptibility signals.

scholarly journals Synthesis, Characterization, Antimicrobial and Anticancer Activity of New Bidentate Schiff Base Ligand and their Transition Metal(II) Complexes

2021 ◽  
Vol 33 (7) ◽  
pp. 1488-1494
Author(s):  
S. Arulmozhi ◽  
G. Sasikumar ◽  
A. Subramani ◽  
A. Sudha ◽  
S.J. Askar Ali
Keyword(s):  
Schiff Base ◽  
Anticancer Activity ◽  
Cell Lines ◽  
Schiff Base Ligand ◽  
Pathogenic Bacteria ◽  
Human Tumor ◽  
Spectral Studies ◽  
Breast Adenocarcinoma ◽  
Human Colon Cancer

The metal(II) complexes were synthesized by addition of corresponding MCl2 (M = Mn2+, Ni2+, Cu2+ and Zn2+) with 1,2-bis(1H-pyrrol-2-ylmethylene)diazane in methanol. The ligand acts as a bidentate as confirmed from the mass, IR, UV, NMR and EPR spectral studies. The Schiff base ligand forms hexa-coordinated complexes having octahedral geometry for Mn(II), Ni(II), Zn(II) and Cu(II) complexes. The metal complexes showed an excellent antimicrobial activity spectrum in vitro against both Gram-negative (Klebsiella pneumoniae and Acinetobacter baumannii), Gram-positive (Staphylococcus aureus and Enterococcus faecalis) and human pathogenic bacteria isolates. To find the binding affinity with protein BSA kinase, for that molecular docking studies were also carried for all the four synthesized metal(II) complexes. The anticancer activity of the synthesized metal(II) complexes was also screened against the three human tumor cell lines MCF7 human breast adenocarcinoma cell line, CaSki human caucasian cervical epidermoid carcinoma and HCT116 human colon cancer cell lines. The present study showed that Zn(II) complex showed potent inhibition by the ratio of 80% as compared to the inhibition in the normal cells (L-6).

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