Resumen

NASUHI PUR, F.  y  AKBARI DILMAGHANI, K.. Synthesis and characterization of new bis-symmetrical adipoyl, terepthaloyl, chiral diimido-di-L-alanine diesters and chiral phthaloyl-L-alanine ester of tripropoxy p-tert-butyl calix[4]arene and study of their hosting ability for alanine and Na⁺. S.Afr.j.chem. (Online) [online]. 2010, vol.63, pp.25-30. ISSN 1996-840X.

Bis-symmetrical tripropoxy p-tert-butyl calix[4]arene esters were prepared from the reaction of tripropoxy calix[4]arene (1HPr₃) with di-acyl chlorides as bridges in the presence of sodium hydride. The esters, which were synthesized from L-alanine acyl chloride derivatives, are optically active. In all of these esters, calix[4]arene cavities have a pinched cone conformation. The structures of these esters were confirmed by FT-IR, ¹H NMR and ¹³C NMR spectroscopy, elemental analysis and ion positive FAB mass spectrometry.

Palabras clave : Synthesis; tripropoxy calix[4]arene; acyl chloride; double calix[4]arenes; L-alanine.

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