Raman Spectra of a Series of Normal Alcohols and Other Compounds

R. W. Wood and George Collins
Phys. Rev. 42, 386 – Published 1 November 1932
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Abstract

The Raman spectra of benzene, cyclohexane, cyclohexene, carbon disulfide, butyl bromide and the normal alcohols from CH3OH to C12H25OH were investigated. The technique recently developed by Wood was used in conjunction with a praseodymium filter. New lines were found in all cases and for some compounds the number was nearly doubled. Two new frequencies at 2660 and 2730 cm1 were found in the spectra of essentially all the alcohols and butyl bromide. They appear to be characteristic of the saturated hydrocarbons. The lines which appear in the Raman spectra of the aliphatic hydrocarbons at 1450 and 1300 cm1 have been attributed respectively to the transverse vibrations of the hydrogens of the CH3 and CH2 groups. The line appearing in the Raman spectra of the alcohols at 1270 cm1 is attributed to the transverse vibrations of the hydrogens of the CH2OH groups. It is pointed out that the Raman spectra of C12H25OH is that of an infinitely long normal alcohol. The new lines of benzene reported by Weiler and Krishnamurti were verified with the exception of the 806 cm1 frequency. In addition a new line at 1690 cm1 was found. The two relatively strong lines of CS2 at 650 and 800 cm1 were each found to be doublet, thus completing the analogy with CO2. The separation of the components in each case was 10 cm1. The existence of a line at 391 cm1, originally reported by Bhagavantam, was verified.

  • Received 14 September 1932

DOI:https://doi.org/10.1103/PhysRev.42.386

©1932 American Physical Society

Authors & Affiliations

R. W. Wood and George Collins

  • Rowland Hall, Johns Hopkins University

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Issue

Vol. 42, Iss. 3 — November 1932

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