Journal of the Chemical Society Faraday Transactions · 1991 · 120 citations · 33 references
Life SciencesBiochemistryCarbohydrate ChemistryMass Spectrometric AnalysisProtein BiochemistryAmino Acid ChemistryAmino Acid CompositionAmino Acid PropertiesPeptide AnalysisPeptide ChemistryAmino Acid AmidesAmino AcidsHeatHeat CapacityHeat Capacity DeterminationPartial Molar Heat CapacityPartial Molar VolumeSolute Partial Molar Properties
Partial molar heat capacities, in water at 25 °C, of the compounds N-acetylglycinamide, N-acetyl-L-alaninamide, N-acetylglycylglycinamide, N-acetylglycyl-L-alaninamide, N-acetyl-L-alanylglycinamide, N-acetyl-L-alanyl-L-alaninamide, glycyl-DL-alanine and DL-alanylglycine have been obtained. The information obtained, for the amides, is discussed in terms of group-additivity approaches, and group contributions are evaluated. The values for these differ in some instances, and particularly that for the heat capacity of the peptide group, from those obtained in an earlier study. Comparison of the parent amino acids and peptides with the amides shows that there is a marked contribution to the heat capacities of the zwitterionic compounds from electrostatic sources.Some results are presented of the partial molar volumes, also at 25 °C, of N-acetylglycyl-L-alaninamide, N-acetyl-L-alanylglycinamide and DL-alanylglycine.A correlation is evident between the heat capacity and volumetric interaction coefficients, for amino acids, peptides and N-acetylamides, obtained from the molality dependences of the apparent molar properties, and this has been rationalised using a simple electrostatic approach.
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