Calixarenes, were introduced in 1870 for the first time but were ignored until 1940. In 1970s they were studied with uncertainty. During 1990 they were presented in brief out line with an emphasize on the use of these molecules for chemical separations. Finally, the discovery of calixarenes was attributed to Zinke (1940) and fully interpreted by Gutsche in 1970. Gutsche was also the first to draw attention to the potential use of them as molecular receptors or enzyme mimics. He proposed that these cyclic oligomers, known as collectively calixarenes in 1978, having recognized in space-filling models of the tetramer a chalice or cup-like shape reminiscent of a Greek crater vase. Baldini et al. 1 in their review paper, illustrated the conformations of calixarenes including: cone, partial cone, 1,2-alternate and 1,3-alternate. Various methods for functionalizing calixarenes have been developed and numerous calixarene derivatives have been synthesized during the past two decades. Various applications of calixarenes are used in purification, chromatography, catalysis, enzyme mimics, ion selective electrodes, phase transfer, transport across membranes, ion channels and self-assembling monolayers 2. Calixarenes have demonstrated outstanding complex ability towards ions, neutral molecules, etc. and are considered as the third best host molecules after cyclodextrins and crown ethers 3. During the last three decades calixarene chromoionophores have long