Structure and conformational equilibrium of thiacalix[4]arene by density functional theory

Density functional theory calculations for the structure and conformational equilibrium of thiacalix4]arene are reported. The conformational equilibrium of thiacalix4]arene, a heterocalixarene in which the phenol groups are bridged by sulphur atoms is compared to the conformational equilibrium of calix4]arene. Thiacalix4]arene conformational energies relative to the cone conformer (ΔE's) are reduced in comparison with calix4]arene. This conformational change is in qualitative agreement with recent NMR spectroscopy measurements of the conformational equilibrium for a tetraethylether of thiacalix4]arene in a CDCl₃ solution which indicates an enhanced chemical exchange of thiacalixarene conformers in comparison with similar methylene bridged structures. Density functional theory results for the structure of thiacalix4]arene are in good agreement with recent X-ray diffraction measurements. The electrostatic potentials in the cone conformers of thiacalix4]arene and calix4]arene suggest that their complexation or recognition abilities can be significantly different. Dipole moments of the four thiacalix4]arene conformers are in the order: cone>1,2-alternate>partial-cone>1,3-alternate.