Photodissociation of dichlorocarbene CCl2 at 248 nm in a cold beam
β Scribed by G.P. Morley; P. Felder; J.Robert Huber
- Publisher
- Elsevier Science
- Year
- 1994
- Tongue
- English
- Weight
- 506 KB
- Volume
- 219
- Category
- Article
- ISSN
- 0009-2614
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β¦ Synopsis
The photodissociation of the dichlorocarbene radical CClz at 248 nm has been studied by photofragment translational speo troscopy. An intense beam of cold CClz was generated from CHCIS by a pulsed molecular beam source equipped with a flash pyrolysis nozzle. The photolysis proceeds exclusively via C-Cl bond fission yielding CC1 + Cl. The photofragment recoil distributions imply that more than 60% of the available energy is channeled into the internal degree of freedom of CC1 and that the angular distribution is almost isotropic.
π SIMILAR VOLUMES
The photodissociation of methyl hydroperoxide (CHaOOH) has been studied in a molecular beam by photofragment translational spectroscopy. As CH,OOH rapidly decomposes upon contact with metal, a new metal-free molecular beam source was designed, which is also suited to the generation of beam pulses of
## Abstract The Br~2~ elimination channel is probed for 1,2βC~2~H~2~Br~2~ in the B${{}^3{\rm{\Pi }}\_{ou}^ + }$βX${{}^1{\rm{\Sigma }}\_g^ + }$ transition upon irradiation at 248 nm by using cavity ringβdown absorption spectroscopy (CRDS). The nascent vibrational population ratio of Br~2~(__v__=1)/B
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