Density functional calculations of oxygen, nitrogen and hydrogen electric field gradient and chemical shielding tensors to study hydrogen bonding properties of peptide group (O C–NH) in crystalline acetamide

• Published in: Journal of molecular graphics & modelling Vol. 26; no. 6; pp. 977 - 981
• Main Authors: Samadi, Z., Mirzaei, M., Hadipour, N.L., Abedini Khorami, S.
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 01.02.2008
• Subjects: Acetamide; Acetamides - chemistry; Crystallization; Deuterium; DFT; Electricity; Hydrogen - chemistry; Hydrogen bond; Hydrogen Bonding; Magnetic Resonance Spectroscopy; Models, Chemical; Nitrogen - chemistry; Nitrogen Isotopes; NMR; Oxygen - chemistry; Oxygen Isotopes; Peptide; Peptides - chemistry; NMR; DFT; Acetamide; Peptide; Hydrogen bond
• ISSN: 1093-3263; 1873-4243
• DOI: 10.1016/j.jmgm.2007.08.003

A density functional theory (DFT) study was carried out to investigate hydrogen bonding (HB) properties of peptide group (O C–NH) in crystalline acetamide. Since the peptide group in acetamide contributes to N–H⋯O and C–H⋯O types of HB interactions, acetamide is considered as the simplest form of peptide linkage in proteins. The evaluated NMR parameters including quadrupole coupling constants and asymmetry parameters from the calculated electric field gradient (EFG) tensors at the sites of O17, N14 and H2 nuclei and isotropic chemical shieldings from the calculated chemical shielding (CS) tensors at the sites of O17, N15 and H1 nuclei reveal the major contribution of O C–NH group to HB interactions. Although N–H⋯O type of HB interaction play the major role in the HB properties of peptide group in lattice form of crystalline acetamide, however, the role of weaker C–H⋯O type of HB interaction cannot be neglected.