Related Experiment Video
Updated: Jul 14, 2026

Palladium N-Heterocyclic Carbene Complexes: Synthesis from Benzimidazolium Salts and Catalytic Activity in Carbon-carbon Bond-forming Reactions
Published on: July 30, 2017
Synthesis, characterization and structure effects on preconcentration and extraction of
Berrin Ziyadanoğullari1, Deniz Ceviziçi, Hamdi Temel
1Faculty of Arts and Sciences, Chemistry Department, Dicle University, Diyarbakir, Turkey. berrinz@dicle.edu.tr
Abstract:
Separation with solvent extraction of Cu(II), Co(II) and Ni(II) from aqueous solution using N,N'-bis-(salicylaldehydene)-1,4-bis-(p-aminophenoxy)butane (H(2)L) as the new extractant has been studied. The new Schiff base, was synthesized by reaction of 1,4-bis-(p-aminophenoxy)butane and salicylaldehyde. Microanalytical data, elemental analysis, UV-vis (1)H NMR and (13)C NMR spectra and IR-spectra were used to confirm the structures. The extractability and selectivity of divalent cations was evaluated as a function of relationship between distribution ratios of the metal and pH or ligand concentration. Cu(+2) showed the highest extractability and selectivity at pH 7.8, whereas Ni(+2) and Co(+2) showed at pH 9.2. From the loaded organic phase, Cu(II), Co(II), Ni(II) stripping were carried out in one stage with aqueous acid solution including various concentrations of HCl. The stripping efficiency was found to be quantitative in case of 1.5M HCl. From quantitative evaluation of the extraction equilibrium data, it has been deduced that the complexes extracted are the simple 1:1 chelates, CuL, CoL, NiL.
More Related Videos
Related Concept Videos
Extraction: Advanced Methods
Qualitative Analysis
For instance, group IV...
Complexation Equilibria: The Chelate Effect
Nucleophilic Aromatic Substitution of Aryldiazonium Salts: Aromatic SN1
In the Sandmeyer reaction, for example, the diazonio group is replaced by a chloro, bromo, or cyano...
Diazonium Group Substitution: –OH and –H
Basicity of Heterocyclic Aromatic Amines

