Magnetic and spectroscopic studies on nickel(II) and copper(II) complexes of some neutral tridentate ONS ligands

1980 ◽  
Vol 58 (7) ◽  
pp. 727-732 ◽  
Author(s):  
M. Akbar Ali

New Schiff base ligands formed from 2-methoxybenzaldehyde and 2,4-dimethoxybenzaldehyde with N-methyl-S-alkyldithiocarbazates and their nickel(II) and copper(II) complexes have been prepared and characterised by elemental analysis and magnetic and spectroscopic measurements. The Schiff bases behave as neutral tridentate chelating agents forming stable nickel(II) complexes of stoichiometry NiLX2•xC2H5OH (L = 2-methoxy- or 2,4-dimethoxybenzaldehyde Schiff bases of N-methyl-S-methyldithiocarbazate; X = I−, SCN−; x = 0, 1). Conductivity, magnetic, and spectral data support an octahedral structure for the nickel(II) complexes. The CuLCl2 complexes were also isolated. Magnetic and spectral evidence are in accord with a chloro-bridged dimeric structure. The chloro-complex of copper(II) with the 2-methoxybenzaldehyde Schiff base displays a room-temperature magnetic moment of 1.81 BM, which remains virtually constant over the temperature range 343–123 K.Hydrated copper(II) chloride promotes complete hydrolysis of the 2,4-dimethoxybenzaldehyde and 2-methoxybenzaldehyde Schiff bases of N-methyl-S-benzyldithiocarbazate with the concomitant formation of copper(II) complexes of the parent N-methyl-S-benzyldithiocarbazate of general formula, Cu(N—SR)Cl2 (R = C6H5CH2—).

1966 ◽  
Vol 19 (12) ◽  
pp. 2241 ◽  
Author(s):  
J Dekkers ◽  
HA Goodwin

Complexes of 1,2-bis(8-quinolylmethyleneimino)ethane with cobalt(II), nickel(II), and copper(II) are described. The copper complexes are five-covalent and, it is suggested, trigonal bipyramidal. Reaction of the Schiff base with iron(II), cobalt(III), and, under certain conditions, nickel(II) leads to its partial hydrolysis, and complexes of the tridentate 1-amino-2-(8-quinolylmethyleneimino)ethane are obtained. The hydrolysis of the Schiff base in the presence of metal ions is discussed in terms of steric effects within the base and of the stereochemical demands of the metal ions. Complexes of 1,2-bis(8-quinolylmethyleneimino)benzene and its hydrolysis derivative 1-amino-2-(8-quinolylmethyleneimino)ethane are also described.


2009 ◽  
Vol 6 (s1) ◽  
pp. S201-S210 ◽  
Author(s):  
Kishor Arora Mukesh Sharma ◽  
Mukesh Sharma ◽  
K. P. Sharma

The studies of 16 new lanthanide(III) nitrate complexes of Schiff base ligands are discussed. Schiff bases were obtained by the condensation of 2–methyl–4–N,N–bis–2' –cyanoethyl aminobenzaldehyde with aniline and 3 different substituted anilines. Lanthanide(III) nitrates,viz. gadolinium(III) nitrate, lanthanum(III) nitrate, samarium(III) nitrate and cerium(III) nitrate were chosen to synthesize new complexes. The complexes were characterized on the basis of physicochemical studiesviz. elemental analysis, spectral,viz. IR and electronic spectral and magnetic studies. TGA studies of some of the representative complexes were also done. Some of the representative complexes were also screened for the anti microbial studies.


2021 ◽  
Author(s):  
SOUMYA SUNDAR MATI ◽  
Dr. SAUGATA KONAR ◽  
BOBY SAMAI

A zinc coordinated rare binuclear complex was synthesised and characterized by elemental analysis and single-crystal X-ray diffraction. Two mononuclear units formed by two Schiff base ligands 2-((2-(pyrimidin-2-yl)hydrazono)methyl)phenol (PHP) coordinated with...


2016 ◽  
Vol 81 (10) ◽  
pp. 1111-1119 ◽  
Author(s):  
Fatemeh Bagheri ◽  
Abolfazl Olyaei

A novel method was developed for synthesizing a series of new three dentate Schiff base ligands starting from hydroxynaphthalidene pyrimidinyl amines with o-phenylenediamines or o-aminophenol or 2-amino-3-hydroxy-pyri-dine in the presence of formic acid catalyst under solvent-free conditions. In these reactions [1+1] condensation product as half-unit ligand was obtained. Moreover, the reaction of hydroxynaphthalidene pyrimidinyl amines with 3,4-diamino-pyridine and 1,8-naphthalenediamine lead to the formation of C2-naphthylated imidazopyridine and dihydropyrimidine, respectively. The attractive features of this protocol are: use of inexpensive catalyst, operationally simple, short reaction times, easy handling, and good yields.


2011 ◽  
Vol 8 (4) ◽  
pp. 1005-1011
Author(s):  
Baghdad Science Journal

Many complexes of 3,5-dimethyl-1H-pyrazol-1-yl phenyl methanone with Cr(III), Co(II), Ni(II), Cu(II) and Cd(II) were synthesized and characterized by FT-IR, UV/visible spectra, elemental analysis, room temperature magnetic susceptibility and molar conductivity. Cd(II) complex was expected to have tetrahedral structure while all the other complexes were expected to have an octahedral structure.


2018 ◽  
Vol 42 (6) ◽  
pp. 4646-4652 ◽  
Author(s):  
Hua Zhang ◽  
Junyang Xing ◽  
Yanhong Dong ◽  
Shangqing Xie ◽  
Shishuai Ren ◽  
...  

The sp2 C–H bond activation of the HCN moiety in diphenylphosphino benzalimines was realized using CoMe(PMe3)4 with the elimination of methane.


2019 ◽  
Vol 48 (33) ◽  
pp. 12496-12511 ◽  
Author(s):  
G. Kalaiarasi ◽  
S. Dharani ◽  
V. M. Lynch ◽  
R. Prabhakaran

Three tetranuclear (1–3) complexes and a mononuclear (4) palladium(ii) complex were synthesized from 3-acetyl-chromen-2-one Schiff base ligands [H2-3MAC-Rtsc] (where R = H; CH3; C2H5[H2-3MAC-etsc] or C6H5) and potassium tetrachloropalladate.


1999 ◽  
Vol 77 (12) ◽  
pp. 2095-2098 ◽  
Author(s):  
Simon J Coles ◽  
Michael B Hursthouse ◽  
David G Kelly ◽  
Andrew J Toner ◽  
Neil M Walker

TiBz4 reacts with N-2-fluorenyl(salicylideneimine) to afford a crystallographically characterized titanium(IV) complex containing two conventional bidentate Schiff base ligands and two O-bound ligands in which the imine function has been reduced by the addition of benzyl and hydrogen moieties.Key words: insertion, nucleophilic additions, Schiff bases, titanium


1988 ◽  
Vol 43 (5) ◽  
pp. 611-615 ◽  
Author(s):  
T. Sogo ◽  
J. Romero ◽  
A. Sousa ◽  
A. de Blas ◽  
M. L. Durán ◽  
...  

Abstract The electrochemical synthesis and physico-chemical properties of neutral zinc(II) complexes of bidentate Schiff bases derived from salicylaldehydes are presented together with the X-ray structure of bis[N-(4-methylphenyl)salicylaldiminato]zinc(II). The crystal is monoclinic, a = 21.877(3), b = 8.801(2), c = 12.027(5) Å, β = 96.55(3)°, space group C2/c. The complex is a monomer, and the zinc atom is tetrahedrally coordinated.


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