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Vibrational relaxation of the N2O ν1 mode

R. T. V. Kung

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Abstract

The vibrational relaxation of the ν1 symmetric stretch mode of N2O was studied at room temperature following an overtone excitation via a DF laser. The ν1 and ν3 (asymmetric stretch) fluorescence at 7.8 and 4.5 μ were, respectively, monitored as a function of time. A V–V equilibration time constant of 0.062 μsec⋅atm between the ν1 and ν2 (bending) modes was measured. The vibrational relaxations out of the ν2 and ν3 modes were measured to be 1.3 and 2.1 μsec⋅atm, respectively, with good agreement compared to previous measurements reported in the literature.

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What this paper is about

The vibrational relaxation of the ν1 symmetric stretch mode of N2O was studied at room temperature following an overtone excitation via a DF laser. The ν1 and ν3 (asymmetric stretch) fluorescence at 7.8 and 4.5 μ were, respectively, monitored as a function of time. A V–V equilibration time constant of 0.062 μsec⋅atm between the ν1 and ν2 (bending) modes was measured. The vibrational relaxations out of the ν2 and ν3 modes were measured to be 1.3 and 2.1 μsec⋅atm, respectively, with good agreement compared to previous measurements reported in the literature.

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Available abstract

The vibrational relaxation of the ν1 symmetric stretch mode of N2O was studied at room temperature following an overtone excitation via a DF laser. The ν1 and ν3 (asymmetric stretch) fluorescence at 7.8 and 4.5 μ were, respectively, monitored as a function of time. A V–V equilibration time constant of 0.062 μsec⋅atm between the ν1 and ν2 (bending) modes was measured. The vibrational relaxations out of the ν2 and ν3 modes were measured to be 1.3 and 2.1 μsec⋅atm, respectively, with good agreement compared to previous measurements reported in the literature.

Key concepts: Overtone, Vibrational energy relaxation, Relaxation (psychology), Excitation, Chemistry, Atomic physics, Bending, Molecular vibration

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