It is shown that for a photon energy of 16.85 eV, the translational energy surprisal of the C2H: +F dissociation products from C2H,F+ has a bimodal hehaviour. The possibility of considering the bimodal surprisal as due to the superposition of two translational energy distributions is consistent with
The appearance energy of C2H+ from C2H2 revisited. A photoion-photoelectron coincidence spectroscopic determination
β Scribed by Ch. Servais; R. Locht
- Publisher
- Elsevier Science
- Year
- 1995
- Tongue
- English
- Weight
- 705 KB
- Volume
- 236
- Category
- Article
- ISSN
- 0009-2614
No coin nor oath required. For personal study only.
β¦ Synopsis
The dissociative ionization of C2H 2 in a C2H+-producing channel has been reconsidered. The photoion-photoelectron coincidence (PIPECO) technique has been used The C2H+/e -coincidence rate curve has been recorded between 16.2 and 21.2 eV. The lowest appearance energy determined for C2 H+ is 17.35 Β± 0.04 eV. A second appearance energy is measured at 18.40 Β± 0.04 Β’V. At both energies ethyny! ions are produced through a predissociation mechanism at the expense of the C2H 2 (A~Ag) state at 17.35 eV and C2H~'(B 2:~ ) at 18.40 eV. These results are in good agreement with the most recent TPIPECO experiments and dissociative electroionization results. This comparison leads to the exclusion of any contribution of autoionization phenomena to the C 2 H + ion production between 16.2 and 21.2 eV. Investigations of C 2 H + through the ion pair formation channel (and the dissociative electron attaci~ment producing C2H-and H-) in C2H 2 are reported and its contribution to C2 H+ ion production below 17.3 eV must be d~scarded.
π SIMILAR VOLUMES
The rotational cutoff levels of C,( B' 'Z:, u" = 1,2), produced in the multiphoton dissociation of jet-cooled acetylene at 193 nm, have been measured using laser-induced fluorescence. This data is used to calculate the values AHf,,(C2) = 194.8iO.5 kcal/ mol and D,(CC-H) = 112.0 kO.8 kcal/mol, in exc
Stark effects were measured for the 2r2-lo1 (85 GHz) and 441-330 (266 GHz) transitions of cyclopropenylidene, C3H2, with a parallel-plate cell designed for transient molecules. From the least-squares analysis of the Stark shifts the dipole moment of &Hz was determined to be 3.43( 2) D, where the err