The infrared and Raman spectra of HCONH2, HCOND2, and an equimolar mix
ture of the two in dimethylsulphoxide (DMSO) at concentrations ranging
from the pure formamide to a very dilute solution have been measured.
The carbonyl stretching band of formamide is asymmetric. At very low
concentrations in DMSO the band becomes symmetric. The behaviour of th
e asymmetry upon dilution can be explained in terms of two ''sites''.
One corresponding to formamide molecules which have no hydrogen bonds
to their carbonyl groups and another to a hydrogen-bonded species form
ing a chain of formamide molecules. The carbonyl stretching band of th
e equimolar mixture does not become symmetric upon dilution. This is b
ecause it consists of the contribution from four different molecules.
Subtraction of the contributions from HCONH2 and HCOND2 produces the s
pectrum of cis- and trans-HCONHD.