Photoelectron spectroscopic study of the oxyallyl diradical

Takatoshi Ichino, Stephanie M. Villano, Adam J. Gianola, Daniel J. Goebbert, Luis Velarde, Andrei M Sanov, Stephen J. Blanksby, Xin Zhou, David A. Hrovat, Weston Thatcher Borden, W. Carl Lineberger

Research output: Contribution to journalArticle

37 Citations (Scopus)

Abstract

The photoelectron spectrum of the oxyallyl (OXA) radical anion has been measured. The radical anion has been generated in the reaction of the atomic oxygen radical anion (O•-) with acetone. Three low-lying electronic states of OXA have been observed in the spectrum. Electronic structure calculations have been performed for the triplet states (3B2 and 3B1) of OXA and the ground doublet state ( 2A2) of the radical anion using density functional theory (DFT). Spectral simulations have been carried out for the triplet states based on the results of the DFT calculations. The simulation identifies a vibrational progression of the CCC bending mode of the 3B2 state of OXA in the lower electron binding energy (eBE) portion of the spectrum. On top of the 3B2 feature, however, the experimental spectrum exhibits additional photoelectron peaks whose angular distribution is distinct from that for the vibronic peaks of the 3B2 state. Complete active space self-consistent field (CASSCF) method and second-order perturbation theory based on the CASSCF wave function (CASPT2) have been employed to study the lowest singlet state (1A1) of OXA. The simulation based on the results of these electronic structure calculations establishes that the overlapping peaks represent the vibrational ground level of the 1A1 state and its vibrational progression of the CO stretching mode. The 1A1 state is the lowest electronic state of OXA, and the electron affinity (EA) of OXA is 1.940 ± 0.010 eV. The 3B2 state is the first excited state with an electronic term energy of 55 ± 2 meV. The widths of the vibronic peaks of the X̃ 1A1 state are much broader than those of the ã 3B2 state, implying that the 1A 1 state is indeed a transition state. The CASSCF and CASPT2 calculations suggest that the 1A1 state is at a potential maximum along the nuclear coordinate representing disrotatory motion of the two methylene groups, which leads to three-membered-ring formation, i.e., cyclopropanone. The simulation of b̃ 3B1 OXA reproduces the higher eBE portion of the spectrum very well. The term energy of the 3B1 state is 0.883 ± 0.012 eV. Photoelectron spectroscopic measurements have also been conducted for the other ion products of the O•- reaction with acetone. The photoelectron imaging spectrum of the acetylcarbene (AC) radical anion exhibits a broad, structureless feature, which is assigned to the X̃ 3A″ state of AC. The ground ( 2A″) and first excited (2A′) states of the 1-methylvinoxy (1-MVO) radical have been observed in the photoelectron spectrum of the 1-MVO ion, and their vibronic structure has been analyzed.

Original languageEnglish (US)
Pages (from-to)1634-1649
Number of pages16
JournalJournal of Physical Chemistry A
Volume115
Issue number9
DOIs
StatePublished - Mar 10 2011

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Photoelectrons
Anions
photoelectrons
anions
Electronic states
Acetone
Binding energy
Excited states
self consistent fields
Electronic structure
Density functional theory
Ions
progressions
acetone
atomic energy levels
Electron affinity
Electrons
Angular distribution
simulation
binding energy

ASJC Scopus subject areas

  • Physical and Theoretical Chemistry

Cite this

Ichino, T., Villano, S. M., Gianola, A. J., Goebbert, D. J., Velarde, L., Sanov, A. M., ... Lineberger, W. C. (2011). Photoelectron spectroscopic study of the oxyallyl diradical. Journal of Physical Chemistry A, 115(9), 1634-1649. https://doi.org/10.1021/jp111311k

Photoelectron spectroscopic study of the oxyallyl diradical. / Ichino, Takatoshi; Villano, Stephanie M.; Gianola, Adam J.; Goebbert, Daniel J.; Velarde, Luis; Sanov, Andrei M; Blanksby, Stephen J.; Zhou, Xin; Hrovat, David A.; Borden, Weston Thatcher; Lineberger, W. Carl.

In: Journal of Physical Chemistry A, Vol. 115, No. 9, 10.03.2011, p. 1634-1649.

Research output: Contribution to journalArticle

Ichino, T, Villano, SM, Gianola, AJ, Goebbert, DJ, Velarde, L, Sanov, AM, Blanksby, SJ, Zhou, X, Hrovat, DA, Borden, WT & Lineberger, WC 2011, 'Photoelectron spectroscopic study of the oxyallyl diradical', Journal of Physical Chemistry A, vol. 115, no. 9, pp. 1634-1649. https://doi.org/10.1021/jp111311k
Ichino T, Villano SM, Gianola AJ, Goebbert DJ, Velarde L, Sanov AM et al. Photoelectron spectroscopic study of the oxyallyl diradical. Journal of Physical Chemistry A. 2011 Mar 10;115(9):1634-1649. https://doi.org/10.1021/jp111311k
Ichino, Takatoshi ; Villano, Stephanie M. ; Gianola, Adam J. ; Goebbert, Daniel J. ; Velarde, Luis ; Sanov, Andrei M ; Blanksby, Stephen J. ; Zhou, Xin ; Hrovat, David A. ; Borden, Weston Thatcher ; Lineberger, W. Carl. / Photoelectron spectroscopic study of the oxyallyl diradical. In: Journal of Physical Chemistry A. 2011 ; Vol. 115, No. 9. pp. 1634-1649.
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AU - Ichino, Takatoshi

AU - Villano, Stephanie M.

AU - Gianola, Adam J.

AU - Goebbert, Daniel J.

AU - Velarde, Luis

AU - Sanov, Andrei M

AU - Blanksby, Stephen J.

AU - Zhou, Xin

AU - Hrovat, David A.

AU - Borden, Weston Thatcher

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N2 - The photoelectron spectrum of the oxyallyl (OXA) radical anion has been measured. The radical anion has been generated in the reaction of the atomic oxygen radical anion (O•-) with acetone. Three low-lying electronic states of OXA have been observed in the spectrum. Electronic structure calculations have been performed for the triplet states (3B2 and 3B1) of OXA and the ground doublet state ( 2A2) of the radical anion using density functional theory (DFT). Spectral simulations have been carried out for the triplet states based on the results of the DFT calculations. The simulation identifies a vibrational progression of the CCC bending mode of the 3B2 state of OXA in the lower electron binding energy (eBE) portion of the spectrum. On top of the 3B2 feature, however, the experimental spectrum exhibits additional photoelectron peaks whose angular distribution is distinct from that for the vibronic peaks of the 3B2 state. Complete active space self-consistent field (CASSCF) method and second-order perturbation theory based on the CASSCF wave function (CASPT2) have been employed to study the lowest singlet state (1A1) of OXA. The simulation based on the results of these electronic structure calculations establishes that the overlapping peaks represent the vibrational ground level of the 1A1 state and its vibrational progression of the CO stretching mode. The 1A1 state is the lowest electronic state of OXA, and the electron affinity (EA) of OXA is 1.940 ± 0.010 eV. The 3B2 state is the first excited state with an electronic term energy of 55 ± 2 meV. The widths of the vibronic peaks of the X̃ 1A1 state are much broader than those of the ã 3B2 state, implying that the 1A 1 state is indeed a transition state. The CASSCF and CASPT2 calculations suggest that the 1A1 state is at a potential maximum along the nuclear coordinate representing disrotatory motion of the two methylene groups, which leads to three-membered-ring formation, i.e., cyclopropanone. The simulation of b̃ 3B1 OXA reproduces the higher eBE portion of the spectrum very well. The term energy of the 3B1 state is 0.883 ± 0.012 eV. Photoelectron spectroscopic measurements have also been conducted for the other ion products of the O•- reaction with acetone. The photoelectron imaging spectrum of the acetylcarbene (AC) radical anion exhibits a broad, structureless feature, which is assigned to the X̃ 3A″ state of AC. The ground ( 2A″) and first excited (2A′) states of the 1-methylvinoxy (1-MVO) radical have been observed in the photoelectron spectrum of the 1-MVO ion, and their vibronic structure has been analyzed.

AB - The photoelectron spectrum of the oxyallyl (OXA) radical anion has been measured. The radical anion has been generated in the reaction of the atomic oxygen radical anion (O•-) with acetone. Three low-lying electronic states of OXA have been observed in the spectrum. Electronic structure calculations have been performed for the triplet states (3B2 and 3B1) of OXA and the ground doublet state ( 2A2) of the radical anion using density functional theory (DFT). Spectral simulations have been carried out for the triplet states based on the results of the DFT calculations. The simulation identifies a vibrational progression of the CCC bending mode of the 3B2 state of OXA in the lower electron binding energy (eBE) portion of the spectrum. On top of the 3B2 feature, however, the experimental spectrum exhibits additional photoelectron peaks whose angular distribution is distinct from that for the vibronic peaks of the 3B2 state. Complete active space self-consistent field (CASSCF) method and second-order perturbation theory based on the CASSCF wave function (CASPT2) have been employed to study the lowest singlet state (1A1) of OXA. The simulation based on the results of these electronic structure calculations establishes that the overlapping peaks represent the vibrational ground level of the 1A1 state and its vibrational progression of the CO stretching mode. The 1A1 state is the lowest electronic state of OXA, and the electron affinity (EA) of OXA is 1.940 ± 0.010 eV. The 3B2 state is the first excited state with an electronic term energy of 55 ± 2 meV. The widths of the vibronic peaks of the X̃ 1A1 state are much broader than those of the ã 3B2 state, implying that the 1A 1 state is indeed a transition state. The CASSCF and CASPT2 calculations suggest that the 1A1 state is at a potential maximum along the nuclear coordinate representing disrotatory motion of the two methylene groups, which leads to three-membered-ring formation, i.e., cyclopropanone. The simulation of b̃ 3B1 OXA reproduces the higher eBE portion of the spectrum very well. The term energy of the 3B1 state is 0.883 ± 0.012 eV. Photoelectron spectroscopic measurements have also been conducted for the other ion products of the O•- reaction with acetone. The photoelectron imaging spectrum of the acetylcarbene (AC) radical anion exhibits a broad, structureless feature, which is assigned to the X̃ 3A″ state of AC. The ground ( 2A″) and first excited (2A′) states of the 1-methylvinoxy (1-MVO) radical have been observed in the photoelectron spectrum of the 1-MVO ion, and their vibronic structure has been analyzed.

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