The B 3Σu- ← b 1Σg+ transition of molecular oxygen

B. R. Lewis; S. T. Gibson; T. G. Slanger; D. L. Huestis

doi:10.1063/1.479056

The B ³Σ_u^- ← b ¹Σ_g⁺ transition of molecular oxygen

B. R. Lewis^*, S. T. Gibson, T. G. Slanger, D. L. Huestis

^*Corresponding author for this work

Research output: Contribution to journal › Article › peer-review

21 Citations (Scopus)

Abstract

The origin of the intensity of the B ³Σ_u^- ← b ¹Σ_g⁺ transition of molecular oxygen, first observed recently by Eppink et al. [J. Chem. Phys. 108, 1305 (1998)], is discussed. It is shown that the B←b transition borrows its intensity principally from the dipole-allowed B←X transition, through spin-orbit mixing between the X ³Σ_g^- and b ¹Σ_g⁺ states. Estimated continuum photoabsorption cross sections and discrete oscillator strengths for the B←b system are presented.

Original language	English
Pages (from-to)	11129-11132
Number of pages	4
Journal	Journal of Chemical Physics
Volume	110
Issue number	23
DOIs	https://doi.org/10.1063/1.479056
Publication status	Published - 15 Jun 1999

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abstract = "The origin of the intensity of the B 3Σu- ← b 1Σg+ transition of molecular oxygen, first observed recently by Eppink et al. [J. Chem. Phys. 108, 1305 (1998)], is discussed. It is shown that the B←b transition borrows its intensity principally from the dipole-allowed B←X transition, through spin-orbit mixing between the X 3Σg- and b 1Σg+ states. Estimated continuum photoabsorption cross sections and discrete oscillator strengths for the B←b system are presented.",

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AU - Lewis, B. R.

AU - Gibson, S. T.

AU - Slanger, T. G.

AU - Huestis, D. L.

PY - 1999/6/15

Y1 - 1999/6/15

N2 - The origin of the intensity of the B 3Σu- ← b 1Σg+ transition of molecular oxygen, first observed recently by Eppink et al. [J. Chem. Phys. 108, 1305 (1998)], is discussed. It is shown that the B←b transition borrows its intensity principally from the dipole-allowed B←X transition, through spin-orbit mixing between the X 3Σg- and b 1Σg+ states. Estimated continuum photoabsorption cross sections and discrete oscillator strengths for the B←b system are presented.

AB - The origin of the intensity of the B 3Σu- ← b 1Σg+ transition of molecular oxygen, first observed recently by Eppink et al. [J. Chem. Phys. 108, 1305 (1998)], is discussed. It is shown that the B←b transition borrows its intensity principally from the dipole-allowed B←X transition, through spin-orbit mixing between the X 3Σg- and b 1Σg+ states. Estimated continuum photoabsorption cross sections and discrete oscillator strengths for the B←b system are presented.

UR - https://www.scopus.com/pages/publications/0001118972

U2 - 10.1063/1.479056

DO - 10.1063/1.479056

M3 - Article

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EP - 11132

JO - Journal of Chemical Physics

JF - Journal of Chemical Physics

IS - 23

ER -

The B ³Σ_u^- ← b ¹Σ_g⁺ transition of molecular oxygen

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