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Synthesis of Macrocyclic Bis-Hydrazone and Their Use in Metal Cations Extraction
Author(s) -
Farouk Kandil,
Mohamad Khaled Chebani,
Wail Al Zoubi
Publication year - 2012
Publication title -
isrn organic chemistry
Language(s) - English
Resource type - Journals
eISSN - 2090-5157
pISSN - 2090-5149
DOI - 10.5402/2012/208284
Subject(s) - hydrazone , dichloromethane , acetylacetone , chemistry , chloroform , extraction (chemistry) , metal ions in aqueous solution , aqueous two phase system , liquid–liquid extraction , aqueous solution , schiff base , metal , proton nmr , carbon 13 nmr , inorganic chemistry , selectivity , polymer chemistry , organic chemistry , catalysis , solvent
Two new macrocyclic hydrazone Schiff bases were synthesized by reaction of succindihydrazide and adipdihydrazide with acetylacetone. Hydrazones have been characterized by elemental analyses and IR, mass, 1 H NMR, and 13 C NMR spectral data. Hydrazones have been studied by liquid-liquid extraction towards the s-metal ions (Li + , Na + , and K + ) and d-metal ions (Cu 2+ and Cr 3+ ) from aqueous phase to organic phase. The effect of chloroform and dichloromethane as organic solvents over the metal chlorides extraction was investigated at 25 ± 0.1°C by using flame atomic absorption. We found differences between the two solvents in extraction selectivity.

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