Abstract
The dynamics of photodissociation of small halogenated alkanes, in both their ground and vibrationally excited states, is investigated. The yield of H, Cl(2P3/2), and Cl(2P1/2) fragments was measured by (2 + 1) resonance-enhanced multiphoton ionization in a time-of-flight mass spectrometer. We report results from the 193 nm photolysis of ground state CHF2Cl, CH3CF2Cl, CH 3CFCl2, and CH3Cl and the 237-243 nm photolysis of CH 3Cl excited to the fourth C-H stretch overtone level. The branching ratios depend on the molecular structure, the accessed excited potential surfaces and, as a consequence, on the dissociation dynamics.
| Original language | English |
|---|---|
| Pages (from-to) | 455-465 |
| Number of pages | 11 |
| Journal | Israel Journal of Chemistry |
| Volume | 37 |
| Issue number | 4 |
| DOIs | |
| State | Published - 1 Jan 1997 |
ASJC Scopus subject areas
- General Chemistry
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