Quinaldine includes shifting hydrogenes which might be involved in
important reactions as the condensation and Mannich reactions.
Quinophtalone has been prepared through the reaction of quinaldine with
phtalyic anhydride in the presence of alumini
um chloride anhydrous
Imines derivatives have been prepared through the reaction of
Quinophtalone with hydroxideamine and phenyl hydrazine and then
diazotion anyhydride has been done to the resulting compounds.
The prepared compounds were characterized by ( H1NMR,IR, MS)
In this research we have synthesized a new macrocyclic Schiff base (II)
containing nitrogen- oxygen donor atoms which was designed and synthesized
by reaction of: 1,4– bis (6',6'- methoxy -3- formyl phenyl)-1,4- dioxa butane (I).
Identification of
this macrocyclic schiff base: (II) 1,16- Diaza–[3,6;11,14-di
(6',6'- methoxy phenyl)]-7,10,19,22 - tetraoxa cyclo tetra icozane-15,1dien was
determined by (LC-MS) and spectroscopy (IR). The liquid- liquid extraction of
metal such as Zn2+, Pb2+ and Ni2+ from aqueous phase to organic phase which
doesn't in water. The effect of chloroform and dichloromethane as organic
solvents over the metal extractions was investigated at 25± 0.10C by using
atomic absorption Spectrometer and extraction percentage was calculated.
This work was focused on the synthesis of tetradentate Schiff bases which
were prepared by condensation of salicylaldehyde with 1,4-diaminobenzene
and 1,3-diaminobenzene. The Schiff base ligands were checked by different
spectral technique (GC-MS,
1H-NMR, IR). The influences of shaking time on
the extraction of Cu (II) using solvent extraction technique was studied. Then
the Kinitic parameters were calculated from schemes which give best line
through drawing log (a-x) vs time or 1/(a-x) vs time or [Cu2+] vs time, whereas
(a-x) represents Cu(II) concentration in water phase and from it (n) reaction
order, (K) reaction rate constant (t1/2) reaction half between prepared ligand
and Cu (II) were calculated.
