An investigation of vibration to rotation transfer in vibrational relaxation of S1 aromatics
โ Scribed by Eric R. Waclawik; Rodney A.J. Borg Mudjijono; Jason R. Gascooke; Christopher G. Hickman; Warren D. Lawrance
- Publisher
- Elsevier Science
- Year
- 1996
- Tongue
- English
- Weight
- 705 KB
- Volume
- 251
- Category
- Article
- ISSN
- 0009-2614
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โฆ Synopsis
A study of vibrational energy transfer for four aromatics with the collision partners H, and He has been undertaken to assess the role of V + R transfer when a low moment of inertia collision partner is involved. Significant transfer occurs to 0' (the only channel for which V + R transfer can occur) in relaxation of benzene and benzene-d, by Hz, but not by He.
For both p-difluorobenzene and toluene there is significant transfer to 0' by both He and Hz, preventing the observation of V -+ R transfer in these polyatomics. It is found that He adopts different pathways when heavy groups are attached to the ring. Hz is more consistent in its preferences.
๐ SIMILAR VOLUMES
ChanSes of the rotaticnal quantum state occurring simultancousi~ (in one arr~k collision step) Edith the deactivation of \_ the torsional vibration ~7 ha%e been measured in $1 OUI IA,. Selscthe ewirarron of rotational Ie\eIs in the vibronic MeI 7' 85s accomplished by means of ;I tunable d> e laser.
The vibrational energy relaxation (VER) of polyatomic molecules has been the central issue in many of the chemical reactions in condensed phase [1][2][3][4][5][6][7][8][9][10][11][12][13][14][15][16][17] as well as in gas phase . The vibrational energy introduced to the molecule is immediately redis
Diffcrential cross sections of thc process Na\*(3 \*P) + M(u = 0) Na(3S) + M(u') have been mcasured for several molecules: Hz, D2, Nz, 02, CO, COz, NzO, Cz H4. WC observe two different types of enerpy spectra. One of them displays il typicalIy non-resonant elcctronic to vibrational energy transfer a
Two anomalous emission bands in the fluorescence spectrum of 3,4-benzpyrenc, dissofvcd in 2.methyfpentane. have been studied 2s a function of temperature. These emissions originate from the second excited singlet state S2. and from ;1 vibrationally excited St state (Sy) respectively. From the temper