Home > Research > Publications & Outputs > Non-dissociative single electron capture by NO2...

Links

Text available via DOI:

View graph of relations

Non-dissociative single electron capture by NO2+ from noble gases

Research output: Contribution to Journal/MagazineJournal articlepeer-review

Published

Standard

Non-dissociative single electron capture by NO2+ from noble gases. / Herman, Z.; Jonathan, P.; Brenton, A.G. et al.
In: Chemical Physics Letters, Vol. 126, No. 2, 01.11.1988, p. 377-384.

Research output: Contribution to Journal/MagazineJournal articlepeer-review

Harvard

Herman, Z, Jonathan, P, Brenton, AG & Beynon, JH 1988, 'Non-dissociative single electron capture by NO2+ from noble gases', Chemical Physics Letters, vol. 126, no. 2, pp. 377-384. https://doi.org/10.1016/0301-0104(88)85045-6

APA

Herman, Z., Jonathan, P., Brenton, A. G., & Beynon, J. H. (1988). Non-dissociative single electron capture by NO2+ from noble gases. Chemical Physics Letters, 126(2), 377-384. https://doi.org/10.1016/0301-0104(88)85045-6

Vancouver

Herman Z, Jonathan P, Brenton AG, Beynon JH. Non-dissociative single electron capture by NO2+ from noble gases. Chemical Physics Letters. 1988 Nov 1;126(2):377-384. doi: 10.1016/0301-0104(88)85045-6

Author

Herman, Z. ; Jonathan, P. ; Brenton, A.G. et al. / Non-dissociative single electron capture by NO2+ from noble gases. In: Chemical Physics Letters. 1988 ; Vol. 126, No. 2. pp. 377-384.

Bibtex

@article{7d576e324da448089a6fe361a711e2f1,
title = "Non-dissociative single electron capture by NO2+ from noble gases",
abstract = "The state-selective non-dissociative single-electron capture reactions of 6 keV NO2+ ions from noble gas (He, Ne, Ar, Kr and Xe) targets are investigated by translational energy spectroscopy. Capture occurs predominantly from ground state NO2+ (X 2Σ+). For the NO+ (X 1Σ+) formation a shift of the peak in the translational energy distribution was found (1.3 to 1.7 eV) which suggests higher vibrational excitation of the molecular product than expected from the mutual position of potential energy curves of the NO system. A simple model assuming a dynamical perturbation of the NO+ curve in the presence of He+ is suggested, which accounts for the shift.",
author = "Z. Herman and P. Jonathan and A.G. Brenton and J.H. Beynon",
year = "1988",
month = nov,
day = "1",
doi = "10.1016/0301-0104(88)85045-6",
language = "English",
volume = "126",
pages = "377--384",
journal = "Chemical Physics Letters",
issn = "0301-0104",
publisher = "Elsevier",
number = "2",

}

RIS

TY - JOUR

T1 - Non-dissociative single electron capture by NO2+ from noble gases

AU - Herman, Z.

AU - Jonathan, P.

AU - Brenton, A.G.

AU - Beynon, J.H.

PY - 1988/11/1

Y1 - 1988/11/1

N2 - The state-selective non-dissociative single-electron capture reactions of 6 keV NO2+ ions from noble gas (He, Ne, Ar, Kr and Xe) targets are investigated by translational energy spectroscopy. Capture occurs predominantly from ground state NO2+ (X 2Σ+). For the NO+ (X 1Σ+) formation a shift of the peak in the translational energy distribution was found (1.3 to 1.7 eV) which suggests higher vibrational excitation of the molecular product than expected from the mutual position of potential energy curves of the NO system. A simple model assuming a dynamical perturbation of the NO+ curve in the presence of He+ is suggested, which accounts for the shift.

AB - The state-selective non-dissociative single-electron capture reactions of 6 keV NO2+ ions from noble gas (He, Ne, Ar, Kr and Xe) targets are investigated by translational energy spectroscopy. Capture occurs predominantly from ground state NO2+ (X 2Σ+). For the NO+ (X 1Σ+) formation a shift of the peak in the translational energy distribution was found (1.3 to 1.7 eV) which suggests higher vibrational excitation of the molecular product than expected from the mutual position of potential energy curves of the NO system. A simple model assuming a dynamical perturbation of the NO+ curve in the presence of He+ is suggested, which accounts for the shift.

U2 - 10.1016/0301-0104(88)85045-6

DO - 10.1016/0301-0104(88)85045-6

M3 - Journal article

VL - 126

SP - 377

EP - 384

JO - Chemical Physics Letters

JF - Chemical Physics Letters

SN - 0301-0104

IS - 2

ER -