Reaction of Bis-(S-Methyl-N-Arylidenehydrazine Carbodithioate)Nickel(II) Chelates With Some Imidazoles
A. M. A Hassaan* and A.K. Abu Al-Nasr
1Chemistry Department, Faculty of Science, Minia University, El-Minta,Egypt. 2Chemistry Department, Faculty of Teachers, Al-Madenha Al-Monwara Abyar Aly, P.O. Box 1343 Saudi Arabia
The addition reactions of imidazole, N-methyl imidazole and 2-methylimidazole as Lewis bases in benzene solution with some bis- (S-methyl-N-arylidenehydrazinecarbodithioate) nickel (II) chelates as Lewis acids have been studied spectrophotornetncally at different temperatures. Stability constants and thermodynamic parameters of the base-adduct formation have been determined and discussed on the light of the different electronic and steric effects of the substituents. It was found that stability of the formed bis-adducts increases as the electron withdrawing strength of the in-plane ligand substituents increases.
KEYWORDS:Imidazoles; Reaction; Reactions; 2-methylimidazole
Download this article as:Copy the following to cite this article: Hassaan A. M. A, Al-Nasr A. K. A. Reaction of Bis-(S-Methyl-N-Arylidenehydrazine Carbodithioate)Nickel(II) Chelates With Some Imidazoles. Orient J Chem 1995;11(3). |
Copy the following to cite this URL: Hassaan A. M. A, Al-Nasr A. K. A. Reaction of Bis-(S-Methyl-N-Arylidenehydrazine Carbodithioate)Nickel(II) Chelates With Some Imidazoles. Orient J Chem 1995;11(3). Available from:http://www.orientjchem.org/?p=37893 |
This work is licensed under a Creative Commons Attribution 4.0 International License.