The title reaction fomls electronically excited HSO6 'A') directly, with considerable vibrational and rotational escitarion as well. The inrernal excitation of the HSO fragment is the maGrnum possible consistent with the concurrenr formation of an O~('A$ molecule as rhc other reaction product. The o
Collision complex formation in the low-energy dynamics of the C+ + O2 reaction
β Scribed by D.M. Sonnenfroh; J.M. Farrar
- Publisher
- Elsevier Science
- Year
- 1986
- Tongue
- English
- Weight
- 645 KB
- Volume
- 125
- Category
- Article
- ISSN
- 0009-2614
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β¦ Synopsis
A crossed beam study of CO+ production from the C+ + 0s reaction at a collision energy of 0.57 eV is presented. Very clear collision complex dynamics are observed which are shown to be consistent with the decay of a transient complex having a lifetime of approximately 0.5 ps. An analysis of the reactive scattering using an adiabatic state correlation diagram indicates that the formation of X-state CO: by insertion of C + into the O2 bond is accessible from the reagents and correlates adiabatically with ground-state products. The average kinetic energy release is approximately 23% of the available energy. A comparison of the present data with the chemiluminescent studies of A-state production of CO* indicates that the dominant channels at low energies are production of ground-state CO+ through the X 211s and a411 u state of COT. ' Alfred P. Sloan Fellow. * Heats of formation are from ref. [ 11, oxygen energy levels from ref. [2].
π SIMILAR VOLUMES
Cross sections for ion formation in'C + 02 collisidns have been measured JS a function of the kinetic energy up to 1.5 eV. Charge transfer is found to g+c rise to C+, O;, C-, 0; and frek electrons. Five processes lading to these ions have been'iden-Med. Reactive ionization is taking place, proceedin
We have studied the quantum dynamics of proton transfer in the hydrogen-bonded complex HaOf-Ha0 using a previously computed three-dimensional potential energy surface. The two coordinates considered are the distance of the hydrogen atom from the O-O midpoint and the O-O distance, for a linear O-H-O
The dependence of the intensity of HeH + particles produced in the title reaction has been measured as a function of scattering angle and product energy. The results exhibit a strong localization in the angle and energy (or velocity) coordinates, which has to be related to crossings of the implied p
CO\*(A "ll-X 2P) emission produced from the C(2P) + O2 reaclm hss been observed al thermal cncrgy III a flowing afterdow apparatus. The relabve vIbrational population In the CO\*(A %I) state was dctcrrnmcd The avcngc fmctlon of VIbntional cncrgy dwrbulcd m CO+(A Zn).(/vJ. ws estimated to be 0.20 i 0