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The High-Resolution Spectra of the ν11 Band of Triacetylene near 622 cm−1: Revised Assignments for Hot Bands

✍ Scribed by S. Haas; G. Winnewisser; K.M.T. Yamada; K. Matsumura; K. Kawaguchi


Publisher
Elsevier Science
Year
1994
Tongue
English
Weight
706 KB
Volume
167
Category
Article
ISSN
0022-2852

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✦ Synopsis


The rovibrational spectra of triacetylene (\left(\mathrm{C}{6} \mathrm{H}{2}\right)) were recorded for the (v_{11}) band in high resolution by FTIR spectroscopy. The assignments for the hot-band system (\left(v_{11}, v_{13}\right)=(1,1) \leftarrow(0,1)) have been fully revised, and reliable molecular parameters have been determined including the rotational and vibrational (l)-type doubling constants. The assignments have been confirmed by a simulation of the absorption profile in the (Q)-branch region. The intensity perturbation caused by the l-type resonance in the (\left(v_{11}, v_{13}\right)=(1,1)) state has been observed and discussed. (c) 1994 Academic Press, Inc.


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The infrared spectrum of monoisotopic \(\mathrm{F}^{35} \mathrm{ClO}_{3}\) has been studied in the region of the \(\nu_{1}\) and \(v_{4}\) bands between 1000 and \(1400 \mathrm{~cm}^{-1}\) with a resolution of ca. \(3 \times 10^{-3} \mathrm{~cm}^{-1}\). Rotational \(J\) and \(K\) structure was obser