FTIR studies of hydrogen bonding between α,β-unsaturated esters and alcohols

• Published in: Journal of molecular structure 1996-06, Vol.379 (1), p.135-142
• Main Authors: Tonge, P.J., Fausto, R., Carey, P.R.
• Format: Article
• Language: English
• Subjects: Alcohol; Carbonyl; Hydrogen bonding; Unsaturated ester
• ISSN: 0022-2860; 1872-8014
• DOI: 10.1016/0022-2860(95)09117-3

The enthalpy (and entropy) of hydrogen bond formation has been measured between the ester carbonyl groups of the two α,β-unsaturated esters thienylacryloyl (TAOMe) and 5-methylthienylacryloyl (5MeTAOMe) methyl ester and the hydrogen bond donors ethanol, phenol and 3,5-dichlorophenol in CCl 4. For the esters, the hydrogen bonding strengths were measured by quantitating the amount of bound and unbound donor, using the OH stretching region, as a function of temperature and applying the van't Hoff equation. The decrease in ν CO of the ester carbonyl group upon hydrogen bond formation Δν CO has also been measured and correlated with the enthalpy of hydrogen bond formation. A linear correlation is observed between the enthalpy of hydrogen bond formation − ΔH and Δν CO, with − ΔH = 1.36 Δν CO − 16.1, where ΔH is measured in kJ mol −1 and Δν in cm −1. Comparison with data for other carbonyl acceptor compounds indicates that the carbonyl group of the above α,β-unsaturated esters is more readily polarized than the carbonyl group of saturated esters or ketones. The quantitative relationship between − ΔH and Δν CO derived here has been used to determine the change in the enthalpy of hydrogen bond formation between substrate and enzyme groups in a series of acylserine proteases.