Experimental and DFT investigation of structure and IR spectra of H-bonded associates of p-(3-carboxy-1-adamantyl)thiacalix[4]arene.

Abstract

The IR spectra of p-(3-carboxy-1-adamantyl)thiacalix[4]arene (1-AdCOOHTC4A) have been studied. IR spectra of crystalline 1-AdCOOHTC4A obtained at room temperature or upon heating to 250°C or its dilute solutions lack bands of free hydroxyl groups. The frequency of hydroxyl groups at 3377cm-1 indicates the formation of an intramolecular H-bond along the lower rim of the 1-AdCOOHTC4A molecule. On the top edge of thiacalixarene, the carboxyl groups form dimeric or cyclic tetrameric complexes via intermolecular H-bonds. The conformation of the cone persists, but there is a mutual influence of H-bonds along the upper and lower rims of the thiacalix[4]arene molecule. The structure with dimer H-bonds between carboxyl groups is 31.9 KJ/mol less preferable than the conformation with tetramer cyclic H-bonds for 1-AdCOOHTC4A. Comparison of the absorption band of νOH alcohol hydroxyl groups in the IR spectra of 1-AdCOOHTC4A at 3377cm-1, with the corresponding band of 1-AdTC4A at 3372cm-1, suggests that the presence of the second system of H-bonds of carboxyl groups in the first molecule does not affect the H-bond of alcohol hydroxyl groups.