Theoretical study of isomerization and dissociation of acetylene dication in the ground and excited electronic states
- 1 October 2005
- journal article
- research article
- Published by AIP Publishing in The Journal of Chemical Physics
- Vol. 123 (13), 134320
- https://doi.org/10.1063/1.2050649
Abstract
Ab initio calculations employing the configuration interaction method including Davidson’s corrections for quadruple excitations have been carried out to unravel the dissociation mechanism of acetylene dication in various electronic states and to elucidate ultrafast acetylene-vinylidene isomerization recently observed experimentally. Both in the ground triplet and the lowest singlet electronic states of C 2 H 2 2 + the proton migration barrier is shown to remain high, in the range of 50 kcal ∕ mol . On the other hand, the barrier in the excited 2 A ″ 3 and 1 A ′ 3 states decreases to about 15 and 34 kcal ∕ mol , respectively, indicating that the ultrafast proton migration is possible in these states, especially, in 2 A ″ 3 , even at relatively low available vibrational energies. Rice-Ramsperger-Kassel-Marcus calculations of individual reaction-rate constants and product branching ratios indicate that if C 2 H 2 2 + dissociates from the ground triplet state, the major reaction products should be CCH + ( Σ − 3 ) + H + followed by CH + ( Π 3 ) + CH + ( Σ + 1 ) and with a minor contribution ( ∼ 1 % ) of C 2 H + ( A 1 2 ) + C + ( P 2 ) . In the lowest singlet state, C 2 H + ( A 1 2 ) + C + ( P 2 ) are the major dissociation products at low available energies when the other channels are closed, whereas at E int > 5 eV , the CCH + ( A ′ 1 ) + H + products have the largest branching ratio, up to 70% and higher, that of CH + ( Σ + 1 ) + CH + ( Σ + 1 ) is in the range of 25%–27%, and the yield of C 2 H + + C + is only 2%–3%. The calculated product branching ratios at E int ≈ 17 eV are in qualitative agreement with the available experimental data. The appearance thresholds calculated for the CCH + + H + , CH + + CH + , and C 2 H + + C + products are 34.25, 35.12, and 34.55 eV. The results of calculations in the presence of strong electric field show that the field can make the vinylidene isomer unstable and the proton elimination spontaneous, but is unlikely to significantly reduce the barrier for the acetylene-vinylidene isomerization and to render the acetylene configuration unstable or metastable with respect to proton migration.This publication has 45 references indexed in Scilit:
- Potential energy surfaces in Coulomb explosion of polyatomic molecules: Benzene and cyclohexane trications and acetylene dicationInternational Journal of Quantum Chemistry, 2005
- Fragment-emission patterns from the Coulomb explosion of diatomic molecules in intense laser fieldsPhysical Review A, 1999
- Study of Unimolecular Reactions by Coulomb Explosion Imaging: The Nondecaying VinylidenePhysical Review Letters, 1998
- A study of the singlet and triplet states of vinylidene by photoelectron spectroscopy of H2C=C−, D2C=C−, and HDC=C−. Vinylidene–acetylene isomerizationThe Journal of Chemical Physics, 1989
- A second order multiconfiguration SCF procedure with optimum convergenceThe Journal of Chemical Physics, 1985
- Structures, energetics and fragmentation pathways of CnH22+ carbodicationsInternational Journal of Mass Spectrometry and Ion Processes, 1985
- Doubly charged ion mass spectra. 7—acetylenesJournal of Mass Spectrometry, 1983
- The structure and stability of the acetylene dicationJournal of Computational Chemistry, 1982
- Doubly charged ion mass spectra: IV—chlorinated and brominated alkanesJournal of Mass Spectrometry, 1982
- The doubly‐charged ion mass spectra of hydrocarbonsJournal of Mass Spectrometry, 1972