Synthesis and characterization of the first phosphonic diamide containing thiazolyl groups: Structural properties and tautomeric equilibrium

Abstract

A new phosphonic diamide containing thiazolyl rings, N, N′ bis(2-thiazolyl) phenylphosphonic diamide, with general formula H 5C 6P(O)[NHCN(CH) 2S] 2 ( 1), was synthesized and characterized by NMR, IR, UV, EI mass-spectrometry and elemental analysis. The X-ray diffraction structure obtained for 1 shows that the crystalline compound exists in the imine form, forming centro-symmetric dimers which are produced by intermolecular cooperative hydrogen bonds leading to a two-dimensional polymeric chain. The preferred tautomeric and conformational equilibria have also been identified in solution. Thus, a tautomeric equilibrium of 97:3% between the amine:imine form is observed in DMSO- d 6. Structural and conformational properties are analyzed using a combined approach involving crystallographic data, vibrational spectra and theoretical calculations at the B3LYP and MP2 (with 6-311++G** and CBSB7 basis sets) level of approximations.