THE PURE ROTATIONAL RAMAN SPECTRUM OF CYCLOPENTANE$^{\ast}$

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1962

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Ohio State University

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The pure rotational Raman spectra of C5H10 and C5H10 were photographed in the 13-th order of a 300 groove mm plane grating using Hg 4358 {\AA} as the exciting line. The spectra are quite weak and diffuse. The line spacing in the S-branches is nearly constant with a value of about 0.864cm−1(C5H10) and 0.644cm−1(C5H10). Transitions with J up to 67 in the ordinary and up to 76 in the deuterated compound were observed in the S-branch. A number of R-branch lines were also observed. The analysis of the spectra is based upon the symmetric rotor theory and yields the rotational constants

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C5H10:Bo=0.21605±0.00010cm−1Do=(5.0±1.4)×10−8cm−1C5D10:Bo=0.16103±0.00013cm−1Do=(4.0/pm2.3)×10−8cm−1$$Assumingaplanarmodelforthecarbonring($D3h$pointgroup)thelengthoftheCCbondis$rCC=1.5373±0.002\AA$ingoodagreementwiththeelectrondiffractionvalueof$1.54\AA1$.Thecyclopentanemoleculeisnot,however,astrictsymmetrictopasisshownbyacarefulanalysisofthethermodynamic$functions2$andthevibrational$spectrum.3$Thepresentstudydoesnotadmitanychoicebetweenthepermissible$C2,C.$,and$C1$symmetries.

Author Institution: Physics Department, Fordham University

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