Pairwise-substitution effects and intramolecular hydrogen bonds in nitrophenols and methylnitrophenols. Thermochemical measurements and ab initio calculations.

The standard molar enthalpies of formation in the gaseous state of a series of nitrophenols, 2-nitrophenol, 3-nitrophenol, 4-nitrophenol, 5-methyl-2-nitrophenol, 2-methyl-5-nitrophenol, and 3-methyl-4-nitrophenol, have been obtained from combustion calorimetry and results from the temperature dependence of the vapor pressure measured by the transpiration method. To verify the experimental data, ab initio calculations of all compounds have been performed using MP, DFT, and G3 methods. Enthalpies of formation derived from the G3 methods are in a good agreement with the experimental results. The quantitative analysis of ortho, meta, and para pairwise-substituent effects in nitrophenols has been performed, and the strength of intramolecular hydrogen bonding in o-nitrophenol has been derived from thermochemical results and compared with those obtained from spectroscopic experiments and ab initio calculations. The new results help to resolve uncertainties in the available thermochemical data on extended series of nitrophenols.