ABSTRACT
The preparation of N-(p-ethylphenyl)thiobenzohydroxamic acid and its spectral properties are described in this paper. The preferred conformation of the acid is investigated by both infrared techniques and theoretical calculations at the DFT level. It is found that the acid exists in the cis thione (Z) form, rather than the trans form (E) in the gas phase. Both infrared spectroscopy and theoretical calculations show that this structure is stabilized by intramolecular hydrogen bonding.
Subject(s)
Hydroxamic Acids/chemistry , Hydroxamic Acids/chemical synthesis , Elements , Molecular Conformation , Spectrophotometry, Infrared , Static Electricity , Stereoisomerism , Thermodynamics , VibrationABSTRACT
The conformational preferences of thiohydroxamic acids (N-hydroxythioamides) are investigated by the density functional B3LYP/6-311++G(3df,3pd)//B3LYP/6-31G(d) method in this work. Unlike hydroxamic acids, the thione and thiol forms are found to be equally stable in the gas phase, and the reaction pathways for the interconversion between the thione and thiol forms have been deduced to involve rotation about the C[double bond, length as m-dash]N bond of the thiol tautomer in the rate-determining step. The effect of aqueous solvation on the reactions has also been investigated. It is found that inclusion of a few explicit water molecules in an implicit solvent calculation is necessary in order to accurately account for hydrogen bonding effects. Thiohydroxamic acids, like their hydroxamic acid analogues, are found to be N-acids, both in the gas phase and in aqueous solution.