Tetrahedron, vol.61, no.44, pp.10443-10448, 2005 (SCI-Expanded)
The synthesis of four diamide derivatives of the p-tert-butylcalix[4]arenes from the reaction of 5,11,17,23-tetra-tert-butyl-25,27-diethoxycarbonylmethoxy- 26,28-dihydroxycalix[4]arene 2 with various primary amines were reported. The 1H and 13C NMR, data showed that the synthesized compounds exist in the cone conformation. The complexing properties of these compounds toward Cr2O72-/HCr2O 7- anions are also studied. It has been observed that receptors 5 and 6 are better extractant than the compounds 3 and 4. The protonated alkyl ammonium form of 5 and 6 is an effective extractant for transferring HCr2O7-/Cr2O 72- anions from an aqueous phase into a dichloromethane layer. © 2005 Elsevier Ltd. All rights reserved.