Molecular hydrogen is observed to be one of the major primary products in the 193 nm photodissociation of phenylstlane. A two-channel dissociation mechanism is proposed, yielding PhSiH + H, and SiH, + PhH with the former predominant. The implications of this observation for experiments which utilise
Photodissociation of acrylonitrile at 193 nm: the CN-producing channel
β Scribed by Cathy A. Bird; D.J. Donaldson
- Publisher
- Elsevier Science
- Year
- 1996
- Tongue
- English
- Weight
- 409 KB
- Volume
- 249
- Category
- Article
- ISSN
- 0009-2614
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β¦ Synopsis
We report the rotational and vibrational quantum state distributions of the CN (X 2,~ +) product formed in the 193 nm photolysis of acrylonitrile (vinyl cyanide). The CN product is formed in v = 0 and v = I with relative populations of 0.86 and 0.14, respectively. The rotational distributions in both v-levels are well fit to a temperature of approximately 1450 K. The results are consistent with a prompt dissociation on the excited electronic potential surface.
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The H atom quantum yield ~b H and the average product translational energy were determined for the HNCO ---, H(2S) + NCO(X 21-I) photodissociation channel at room temperature for a photolysis wavelength of 193 nm. HNCO was photolyzed using an ArF excimer laser and nascent H atoms were detected by va
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