Citation

By A, Neville GA, Shurvell HF. J. Forensic Sci. 1992; 37(2): 503-512.

Affiliation

Bureau of Drug Research, Health Protection Branch, Health and Welfare Canada, Ottawa, Ontario.

Copyright

(Copyright © 1992, American Society for Testing and Materials, Publisher John Wiley and Sons)

DOI

unavailable

PMID

1500895

Abstract

Fourier transform Raman and infrared spectra of pure cis(Z)- and trans(E)-2,5-dimethoxy-4,beta-dimethyl-beta-nitrostyrene (precursors of the psychotomimetic street drug STP or DOM) were recorded in the solid state. The spectra show characteristic features of the ethylene moiety and of the aryl and nitro substituents which permit ready differentiation and identification of these isomers. A very strong Raman line at 1670 cm-1 from the cis isomer for the C=C stretching mode, in comparison with a strong Raman line at 1641 cm-1 for the trans isomer, affords primary differentiation of these substances. A second characteristic, of both the Raman and infrared (IR) spectra, is that the frequency of the strong symmetric nitro (NO2) stretching band is about 40 cm-1 higher in the cis (1346 cm-1) than the trans isomer (1301 cm-1). All major IR and Raman bands are reported and given vibrational assignments.

Language: en