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  Rotational Raman Spectroscopy
The Raman Effect page 4 of 4
   
Practical Navigator
Introduction
The Raman Effect
Experimental Techniques
1. Rotational Raman Spectroscopy
Interpreting the Spectrum
Effect of Bond Length
Centrifugal Distortion
Intensities of Spectral Lines
Nuclear Spin Statistics
2. Real Diatomic Molecules
Temperature
Spectrum of Nitrogen
Isotopic Substitution
Nuclear Spin Statistics
Predict the Spectrum of Oxygen
 
_J = 0, J = ±2 (8)

_J = 0 transitions correspond to the intense Rayleigh scattering.

Thus if the molecule gains rotational energy from the photon during collision, a series of S branch lines is apparent to low wavenumber side of the exciting line which are called Stokes lines. An S-branch can also be formed on the Anti-Stokes side of the excitation line.

Q If Stokes transitions form an S branch, how can Anti-Stokes transitions be labelled S as well?

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