The solvent extraction of Fe3+ cations from the aqueous to the organic (chl
oroform) phase was carried out using p-tert-butyl calix[4]arene((1) under b
ar), calix[4]arene((2) under bar), diazo-coupling calix[4]arenes [p-(4-n-bu
tylphenylazo)calix[4]arene ((3) under bar), p-(4-phenylazophenylazo)calix[4
]arene((4) under bar), p-(4-acetanilidazo)calix[4]arene((5) under bar), p-(
N'-2-thyazol-2ylsulphanylazo)calix[4]arene((6) under bar) and p-(2-thyazola
zo)calix[4]arene((8) under bar) and the derivatives of phenol [2-(5-bromo-2
-pyridylazo)-5-diethylaminophenol((8) under bar) (Bromo-PADAP) and 2-hydrox
y-5-methylphenylazonapthol((9) under bar) (HMPAN)]. It was found that the c
ompounds ((1) under bar-(9) under bar) showed the highest extractability to
ward Fe3+ at pH 4.5-5.4 Compound (5) under bar shows strong binding ability
to Fe3+ ion. Based on the method of continuous variation, calixarene 5 for
med a 1:1 complex with Fe3+ ion.