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Photofragmentation of NOCl in a molecular beam at 193 nm: a bimodal vibrational state distribution

โœ Scribed by B.-M. Haas; P. Felder; J. Robert Huber


Publisher
Elsevier Science
Year
1991
Tongue
English
Weight
673 KB
Volume
180
Category
Article
ISSN
0009-2614

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โœฆ Synopsis


The 193 nm photodissociation of NOCI has been studied by photofragment translational spectroscopy under collisionless conditions, Time-of-flight (TOF) distributions of the Cl and NO fragments were measured at various detectton angles and different laser polarizations. The overall vibrational distribution of the NO fragments was found to extend from u" =O to, at least, 0" =24, wnsistmg of two distributions, both centered at around v" = 15. The broad distribution (AU" c 24), having a recoil anisotropy flcO.45, and the narrow one (AU' ~8) with p=O.95, emerge from different reaction channels, i.e. potential energy surfaces of NOCI which evince different vibrational coupling strengths. The results are interpreted in terms of an initial excitation of two close-lying electronic states of A' symmetry.


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โœ M.-A. Thelen; P. Felder; J. Robert Huber ๐Ÿ“‚ Article ๐Ÿ“… 1993 ๐Ÿ› Elsevier Science ๐ŸŒ English โš– 604 KB

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