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1 H NMR spectra part 31 : 1 H chemical shifts of amides in DMSO solvent
Author(s) -
Abraham Raymond J.,
Griffiths Lee,
Perez Manuel
Publication year - 2014
Publication title -
magnetic resonance in chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.483
H-Index - 72
eISSN - 1097-458X
pISSN - 0749-1581
DOI - 10.1002/mrc.4079
Subject(s) - chemical shift , chemistry , steric effects , solvent , solvent effects , proton , hydrogen bond , amide , nmr spectra database , computational chemistry , crystallography , spectral line , molecule , stereochemistry , organic chemistry , physics , quantum mechanics , astronomy
The 1 H chemical shifts of 48 amides in DMSO solvent are assigned and presented. The solvent shifts Δ δ (DMSO‐CDCl 3 ) are large (1–2 ppm) for the NH protons but smaller and negative (−0.1 to −0.2 ppm) for close range protons. A selection of the observed solvent shifts is compared with calculated shifts from the present model and from GIAO calculations. Those for the NH protons agree with both calculations, but other solvent shifts such as Δ δ (CHO) are not well reproduced by the GIAO calculations. The 1 H chemical shifts of the amides in DMSO were analysed using a functional approach for near ( ≤ 3 bonds removed) protons and the electric field, magnetic anisotropy and steric effect of the amide group for more distant protons. The chemical shifts of the NH protons of acetanilide and benzamide vary linearly with the π density on the α N and β C atoms, respectively. The C=O anisotropy and steric effect are in general little changed from the values in CDCl 3 . The effects of substituents F, Cl, Me on the NH proton shifts are reproduced. The electric field coefficient for the protons in DMSO is 90% of that in CDCl 3 . There is no steric effect of the C=O oxygen on the NH proton in an NH…O=C hydrogen bond. The observed deshielding is due to the electric field effect. The calculated chemical shifts agree well with the observed shifts (RMS error of 0.106 ppm for the data set of 257 entries). Copyright © 2014 John Wiley & Sons, Ltd.