A procedure has been developed to permit recalculation of a Raman spectrum
that has been taken on a source spectrometer to allow its quantitative use
with data taken from a target system. The procedure is based on accurate ch
aracterization of both the source and target spectral abscissas by means of
a neon spectrum that Is recorded at the time the Raman measurements are ma
de. Corrections are made for wavelength-dependent behavior of both systems,
for differences in dispersion for the two systems, and for variation in th
e number, spacing, and size of the detector elements. An example Is present
ed in which the fingerprint and CH regions of the Raman spectrum of cyclohe
xane are transferred from higher to lower resolution context.