ELUCIDATING THE ORIGIN OF CONFORMATIONAL ENERGY DIFFERENCES IN SUBSTITUTED 1,3-DIOXANES - A COMBINED THEORETICAL AND EXPERIMENTAL STUDY

摘要

C-13 NMR spectroscopy, ab initio quantum mechanics, and molecular mechanics have been used to investigate the trans-4-(trifluoromethyl)-2, 2, 6-trimethyl-1, 3-dioxane chair/twist-boat equilibrium. The molecular mechanics calculations were based upon the MM3 and AMBER force fields. A 61-31G* basis was used for the ab initio calculations, and MP2 correlation corrections were applied. Both the ab initio and AMBER molecular mechanics calculations are consistent with the C-13 NMR chemical shift differences for the trans-4-(trifluoromethyl)-2, 2, 6-trimethyl-1, 3-dioxane conformers. The predicted chair to twist-boat equilibrium suggested by the MM3 calculations is not consistent with the experimental data. These results support the suggestion by Howard et al. (Howard, A. E; Cieplak, P.; Kollman, P. A. J. Comput Chem. 1995, 16, 243-261) on the critical role of electrostatic interactions in determining the chair/twist-boat equilibrium. [References: 15]