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Infrared and Raman spectra of aminothiazolides (phenylacetamides of glycine) and their diazo derivatives, a series of NH-CS-CH2-NH-CS-CH2-CO-R, were measured in the region of 1800-100 cm-1. The frequencies of the ring hydrogen-hydrogen stretching mode, the carbonyl mode, and the geminal formyl vibration were determined. They are rationalized in terms of a spectroscopic model of an equilibrated structure in which the CO and NH-CS-CH2-CO groups are at 90 degrees or in the anti-conformation with respect to the CS-CH2-NH moiety. Vibrations of the phenyl ring are not significantly perturbed by the replacement of the amido-NH-CS-CH2-CO group with an amido-CO-CH2-NH group. The carbonyl formyl vibration is not significantly perturbed either by the nature of the leaving group (Cl, Br, F) or by the presence of an N-methyl moiety in the amido function.Q
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