## Received17Aprill99l;infinalform 15May 1991 Mass and kinetic energy resolved Ar: ions have been photodissociated at 532 nm in the entrance to a 2 m time-of-flight device. Subsequent deflection of all the ions allows for time resolved measurements to be undertaken on the neutral photofragments. A
Photodissociation of Ar+3 cluster ion
β Scribed by Takashi Nagata; Jun Hirokawa; Tsutomu Ikegami; Tamotsu Kondow; Suehiro Iwata
- Publisher
- Elsevier Science
- Year
- 1990
- Tongue
- English
- Weight
- 561 KB
- Volume
- 171
- Category
- Article
- ISSN
- 0009-2614
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β¦ Synopsis
The time-of-flight spectra of Ar+ produced in the photodissociation of Ar: were observed in the wavelength range of 460-590 nm. Analysis revealed that (I ) the kinetic energy distribution of Ar* fragments is bimodal: the components having a released kinetic energy of x0.5-1.0 eV (fast component) and almost zero kinetic energy (slow component), ( ) the fragment angular distribution displays an anisotropy characteristic of direct dissociation involving a parallel-type transition, and (3 ) the formation of the fast component is the dominant channel with a branching fraction more than 80%. A dissociation mechanism involving a linear symmetric precursor is proposed on the basis of ab initio calculations for the potential energy surfaces of Ar:.
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New ab initio calculations are reported that indicate Art is a linear, asymmetric, C, molecule with equilibrium bond lengths R, ~2.47 A and R2= 2.73 A. The potential energy surface is very shallow along the asymmetric stretch coordinate indicating excursions of the least bound argon atom of 0.5 to 0
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