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The pure rotational Raman spectrum of acetylene has been recorded with argon laser excitation and a resolution of about 0.3 cm −1 . For the first time ΔJ = 1 transitions in the excited II states are clearly resolved up to J = 9. Formulae for the intensity distribution in rotational Raman spectra of linear molecules in the ground and vibrational II states have been derived including the effect of I ‐type doubling. After a qualitative discussion these formulae are applied to a quantitative analysis of the acetylene spectrum.
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Finsterhölzl et al. (1977) studied this question.
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