Abstract:
A wide variety of acyclic ureas comprising alkyl, arylalkyl, acyl, and aryl functional groups are investigated
by nuclear magnetic resonance spectroscopy. In general, spectral characteristics of more than 130 substances
based on acyclic ureas dissolved in deuterated dimethyl sulfoxide at room temperature are studied. The results
obtained based on the studies of 1H and 13C NMR spectra of urea and its N-alkyl-, N-arylalkyl-, N-aryland
1,3-diaryl derivatives are presented, and the effect of these functional groups on the chemical shifts in
carbonyl and amide moieties in acyclic urea derivatives is discussed. An introduction of any type of substituent
(electron-withdrawing or electron-donating) into urea molecule is stated to result in a strong upfield shift
in 13C NMR spectra relatively to unsubstituted urea. A strong sensitivity of NH protons to the presence of
acyl and aryl groups in nuclear magnetic resonance spectra is pointed out. In some cases, qualitative dependencies
between the chemical shifts in the NMR spectra and the structure of the studied acyclic ureas are revealed.
A summary of the results on chemical shifts in the NMR spectra of the investigated substances allows
determining the ranges of chemical shift variations of the key protons and carbon atoms in acyclic ureas. The
literature describing the synthesis procedures are provided. The results obtained significantly expand the
methods of reliable identification of biologically active acyclic ureas and their metabolites that makes it
promising to use NMR spectroscopy both in biochemistry and in clinical practice.
