Synthesis of cesium selective pyridyl azocalix[n]arenes

A series of pyridylazo calixn]arenes (n=4, 6, 8) including the first examples of mixed hetroaryl azocalix(n)arenes have been synthesized by coupling calixn]arenes with diazonium salts derived from amino pyridines. It has been observed that the coupling reaction of diazonium salt obtained from 3-aminopyridine with calixn]arene gives tetrakis-, hexakis- and octakis (pyridylazo)calixn]arenes (n=4,6,8) while those derived from 4-aminopyridine give partially substituted (4-pyridylazo)calixn]arene analogs. There is no reaction of calix(n)arenes with diazonium salts derived from 2-aminopyridine under identical conditions of experiments. The conformational analysis of synthesized compounds have been ascertained by detailed spectral measurements and single crystal X-ray analysis of 5-(3′-pyridylazo)-25,26,27,28-tetrahydroxycalix4]arene. A rational explanation for the observed partial and exhaustive coupling reaction in the synthesis of heteroaryl azocalix(n)arenes has been suggested. Preliminary evaluation of synthesized derivatives as molecular receptors for metal ions indicates that they have good potential to function as selective ionic filters for cesium ions.