Stability and structure of the C2H6+ion: investigation of the photoelectron spectrum of ethane below 14 eV usingab initiomethods
- 1 May 1977
- journal article
- research article
- Published by Taylor & Francis in Molecular Physics
- Vol. 33 (5) , 1345-1366
- https://doi.org/10.1080/00268977700101121
Abstract
Potential surfaces have been calculated for ethane and the three lowest-lying states of its positive ion using ab initio SCF and CI methods. The C2H6 + states treated consist of two 2 Ag and a single 2 Bg species in the lowest nuclear symmetry considered (C 2h ) and they are found to possess markedly different equilibrium structures both compared to ethane itself and also to one another. The C2H6 + ground state (2 Ag ) is a pure 2 A 1g species (D 3d symmetry) at large CC distances with optimum CCH angles of 100°, but at shorter R CC values it becomes a mixture of both 2 A 1g and 2 Eg character through a large diborane-type (v 12) distortion. The second 2 Ag species is complementary to the first and appears to prefer D 3d symmetry both at large CC values, for which it is a 2 Eg species, and also at short distances, for which it eventually becomes a 2 A 1g state. The 2 Bg species correlates with 2 Eg in D 3d symmetry but is Jahn-Teller distorted, possessing an R CC value of 2·75 bohr and an HCH angle of only 90° (ethane values are 2·91 bohr and 109·47°). A Franck-Condon analysis of the calculated potential curves indicates that the spectrum for ionization to the lowest 2 Ag species is too diffuse and of wrong characteristic frequency to be attributed to the fairly regular fine structure observed in the 11·5–12·6 eV region of the ethane PES (with average vibrational spacting of 1170 cm-1). By contrast the analogous results for 2 Bg ionization do compare quite well with the latter experimental system, with both the v 3 (CC stretch) and v 11 (CH3 deformation) modes showing progressions in the desired frequency range. Finally it is argued that a breakdown of the Born-Oppenheimer Approximation for the 2 Ag states in the region of vertical ionization coupled with the fact that one of the species dissociates in the same energy region is responsible for the much more irregular and broad appearance of the PES observed in the 12·5–14·0 eV region.Keywords
This publication has 27 references indexed in Scilit:
- AB initio vibrational analysis of the Schumann—Runge bands and the neighboring absorption region of molecular oxygenChemical Physics Letters, 1976
- Ab initio calculations on the electronic spectrum of ethaneChemical Physics, 1975
- Electronic states of C2H6+Molecular Physics, 1974
- Electronic spectra of paraffin hydrocarbonsMolecular Physics, 1972
- Vibrational analysis of the electronic spectrum of ethylene based onab initio SCF-CI calculationsTheoretical Chemistry Accounts, 1972
- Photoelectron spectroscopic correlation of the molecular orbitals of methane, ethane, propane, isobutane and neopentaneJournal of the Chemical Society, Faraday Transactions 2: Molecular and Chemical Physics, 1972
- Unparameterized localized orbital calculations for saturated hydrocarbonsChemical Physics Letters, 1971
- The electronic configurations of alkanes studied by high resolution photoelectron spectroscopyJournal of Molecular Structure, 1971
- Theory of the ionization of ethaneMolecular Physics, 1971
- Calculated ionization potentials of the linear alkanesMolecular Physics, 1970