Rate constants for the reactions of atomic oxygen ( 0 3 P ) with C&3F, C&IaCl,C@3Br, 1, l-CzHzFz, and I ,2-C&IzFz have been measured at 307' K using a discharge-flow system coupled to a mass spectrometer. The rate constants for these reactions are (in units of 1011cm3mole-1s-1)2.63 &0.38,5.22 =tO0.2
Quantal and semiclassical studies of the (CO2) laser-induced reaction: F(2P1/2) + H2 → [F(2P3/2) + H2; HF + H]
✍ Scribed by Michael Baer; Isidore Last; Yaakov Shima
- Publisher
- Elsevier Science
- Year
- 1984
- Tongue
- English
- Weight
- 436 KB
- Volume
- 110
- Category
- Article
- ISSN
- 0009-2614
No coin nor oath required. For personal study only.
✦ Synopsis
In this work we studied the collinear F(*P,$ + Hz system in a strong CO2 laser field. It was found that the tiajecror) surface hopping method (TSHM) yields entirely different results than the exact quantum-mechanical treatment. A curvecrossing model was devised to esplain the discrepancy.
📜 SIMILAR VOLUMES
The collinear F(zPs/2, zPr$ + Ha system in a strong laser field is studied, employing the trajectory-surface-hopping method. The results are compared with a recent quanta1 study by Zimmerman, Baer and George. The two treatments yield low electronic non-adiabatic transition probabilities (~0.1). Good
2-fluorovinyl radicals were generated in solid argon by solid-state chemical reactions of mobile F atoms with acetylene and its deuterated analogues. Highly resolved EPR spectra of the stabilized radicals CHF&dbond(\*)CH, CDF&dbond(\*)CD, CHF&dbond(\*)CD, and CDF&dbond(\*)CH were obtained for the fi
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## Abstract Quantum mechanical wave packet calculations are carried out for the H(^2^S) + FO(^2^II) → OH(^2^II) + F(^2^P) reaction on the adiabatic potential energy surface of the ground ^3^__A__″ triplet state. The state‐to‐state and state‐to‐all reaction probabilities for total angular momentum _