scholarly journals Studies of Some Lanthanide(III) Nitrate Complexes of Schiff Base Ligands

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.

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—).


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...


1974 ◽  
Vol 29 (7-8) ◽  
pp. 565-566 ◽  
Author(s):  
R. N. Prasad ◽  
J. P. Tandon

The magnetic susceptibilities of some newly syntesized Al(III) and Si(IV) complexes of Schiff bases derived from the condensation of o-hydroxyacetophenone or 2-dydroxy-1-naphthaldehyde with hydroxyalkylamines or diamines have been measured and the data indicate their diamagnetic character.


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.


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.


1997 ◽  
Vol 4 (2) ◽  
pp. 65-68 ◽  
Author(s):  
Zahid H. Chohan ◽  
Syed K. A. Sherazi

Metal(II) complexes of hydrazine derived Schiff-base ligands of the type M(L)2Cl2 where M = Co, Cu, Ni and Zn and L = L1 and L2 have been prepared and characterised by molar conductance, magnetic moment, elemental analysis and electronic, IR, H-NMR and C13 spectral data.The different modes of chelation of the ligands and their comparative biological properties against different bacterial species are reported.


1973 ◽  
Vol 26 (7) ◽  
pp. 1459 ◽  
Author(s):  
WW Fee ◽  
JD Pulsford ◽  
PD Vowles

The kinetics of copper(II)-promoted solvolyses of two series of nickel(II) complexes containing polydentate Schiff bases with various remote substituents, in dimethyl sulphoxide (dmso), are discussed from the viewpoints of rate constants and of enthalpies and entropies of activation. Appearance of an isokinetic relation for the tridentate (ONS donors) reactants may indicate a common mechanism operative within this reactant series. Rate constants appear related to σp values in such a way that a dissociative mechanism appears important for the tridentate reactants, while characterization in terms of associative behaviour is indicated for the tetradentates.


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