HIGH-RESOLUTION VIBRATION-ROTATION SPECTROSCOPY OF SUBSTITUTED $METHANES^{*}$

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1981

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Ohio State University

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The vibration-rotation spectrum of the v2 and v5 fundamentals of CDF3, the v1 fundamental of CBrF3, and the v4 fundamental of CD4 have been recorded using a Nicolet 7199 Fourier Transform Infrared Spectrometer. In addition, the Q-branch and several R(J) and P(J) sub-bands of each of these transitions have been investigated using a tunable semiconductor diode laser spectrometer. In v2(CDF3), the Q-branch and the K-structure in the P(J) subbands are resolved and assigned for the first time. Constants derived for this band are (in cm−1) \begin{eqnarray*} v_{2} = 1111.1823_{6} \quad \alpha_{2}^{B} = 0.001646_{11} \quad D_{\alpha}^{J} = (2.5+0.5) \times 10^{-7} \ A_{2} =0.018623_{4} \quad \alpha{ _{2}}^{A}- \alpha _{2}^{B} = 0.001238_{9} \quad D_{2}^{J} = (3.4+0.5) \times 10^{-7}; \\ B_{2} = 0.32928_{2} \quad D_{2}{^{J}} =D_{D}{^{J}} = (9+4) \times 10^{-8} \end{eqnarray*} these are nearly 100 times more precise than those reported in previous work.1 Improved constants will also be reported for CBrF3 and CD4.

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Supported by the National Science Foundation. 1N.J. Fyke, P. Lockett, J.K. Thompson, and P. M. Wilt, J. Mol. Spectroscopy 58, 87 (1975).


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