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
Time-resolved FTIR studies of the photodissociation of pyruvic acid at 193 nm
โ Scribed by Gregory E. Hall; James T. Muckerman; Jack M. Preses; Ralph E. Weston Jr.; George W. Flynn
- Publisher
- Elsevier Science
- Year
- 1992
- Tongue
- English
- Weight
- 657 KB
- Volume
- 193
- Category
- Article
- ISSN
- 0009-2614
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โฆ Synopsis
Infrared emission from carbon dioxide produced in the 193 nm photolysis of pyruvic acid vapor has been investigated using time-resolved Fourier transform infrared spectroscopy as a probe. A broad feature, strongly red-shifted from the antisymmetric stretching fundamental (Y,) of CO*, dominates the early spectrum. A statistical model using a linear surprisal is shown to provide good agreement with the observed spectral contour, but only if the energy available to the photofragments corresponds to the direct formation of acetaldehyde along with COz.
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## With minor modifications to commercial instrumentation, time-resolved FTIR emission spectroscopy is demonstrated for the determination of photofragment internal state distributions. Vinyl chloride and dichloroethylene photolysis at 193 nm serve as test cases and exhibit high signal-to-noise.
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