Intramolecular V-V transfer between the components of the (31/214151) and (3141/214251) Fermi dyads in acetylene in C2H2-C2H2 collisions

Sarah Henton, Meez Islam, Ian W.M. Smith

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Abstract

Infrared-ultraviolet double resonance experiments have been performed to determine rate coefficients for collisional intramolecular vibration-vibration transfer in pure acetylene within two Fermi dyads: (a) that formed from almost equal mixtures of the zero-order, normal-mode states |31〉 and |21(4151)0〉 and (b) that which is composed predominantly of the |3141 1〉, |2142 251 -1〉 and |2142 051 1〉 states. Pulses of tunable IR excited molecules to the lower component (II) of one of the Fermi dyads and the evolution of population in the upper component (I) was observed by exciting laser-induced fluorescence (LIF) from this level using tunable UV laser radiationIn this Letter, we employ the notation for vibrational states whereby, for example, 31 denotes one quantum of excitation in the ν3 normal mode. (31/214151)I, II denotes the Fermi dyad in which the principal contributions to the vibrational eigenstates are from the normal mode wavefunctions describing the zeroth-order 31 fundamental and 214151 combination vibrational states. In each dyad, the subscript II is used to denote the lower of the two component states, I the higher. Analysis of the LIF signals vs. time yields the following rate coefficients (kid) for intradyad transfer at 295 K: for (31/214151)I↔II, kid=(2.1±0.2)×10-10 cm3 molecule-1 s-1; for (3141/214251)I↔II, kid=(3.2±0.6)×10-11 cm3 molecule-1 s-1. These results are discussed in terms of the matrix elements for such collision-induced transitions and differences in the mixing of the zero-order states in these two pairs of Fermi dyads.

Original languageEnglish
Pages (from-to)223-230
Number of pages8
JournalChemical Physics Letters
Volume291
Issue number1-2
DOIs
Publication statusPublished - 10 Jul 1998

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Acetylene
acetylene
vibrational states
laser induced fluorescence
Molecules
collisions
Lasers
Fluorescence
molecules
vibration
coefficients
Wave functions
tunable lasers
ultraviolet lasers
eigenvectors
coding
Infrared radiation
matrices
pulses
excitation

Cite this

@article{249a34e8d1484c4b926f412905312fb3,
title = "Intramolecular V-V transfer between the components of the (31/214151) and (3141/214251) Fermi dyads in acetylene in C2H2-C2H2 collisions",
abstract = "Infrared-ultraviolet double resonance experiments have been performed to determine rate coefficients for collisional intramolecular vibration-vibration transfer in pure acetylene within two Fermi dyads: (a) that formed from almost equal mixtures of the zero-order, normal-mode states |31〉 and |21(4151)0〉 and (b) that which is composed predominantly of the |3141 1〉, |2142 251 -1〉 and |2142 051 1〉 states. Pulses of tunable IR excited molecules to the lower component (II) of one of the Fermi dyads and the evolution of population in the upper component (I) was observed by exciting laser-induced fluorescence (LIF) from this level using tunable UV laser radiationIn this Letter, we employ the notation for vibrational states whereby, for example, 31 denotes one quantum of excitation in the ν3 normal mode. (31/214151)I, II denotes the Fermi dyad in which the principal contributions to the vibrational eigenstates are from the normal mode wavefunctions describing the zeroth-order 31 fundamental and 214151 combination vibrational states. In each dyad, the subscript II is used to denote the lower of the two component states, I the higher. Analysis of the LIF signals vs. time yields the following rate coefficients (kid) for intradyad transfer at 295 K: for (31/214151)I↔II, kid=(2.1±0.2)×10-10 cm3 molecule-1 s-1; for (3141/214251)I↔II, kid=(3.2±0.6)×10-11 cm3 molecule-1 s-1. These results are discussed in terms of the matrix elements for such collision-induced transitions and differences in the mixing of the zero-order states in these two pairs of Fermi dyads.",
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Intramolecular V-V transfer between the components of the (31/214151) and (3141/214251) Fermi dyads in acetylene in C2H2-C2H2 collisions. / Henton, Sarah; Islam, Meez; Smith, Ian W.M.

In: Chemical Physics Letters, Vol. 291, No. 1-2, 10.07.1998, p. 223-230.

Research output: Contribution to journalArticle

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AB - Infrared-ultraviolet double resonance experiments have been performed to determine rate coefficients for collisional intramolecular vibration-vibration transfer in pure acetylene within two Fermi dyads: (a) that formed from almost equal mixtures of the zero-order, normal-mode states |31〉 and |21(4151)0〉 and (b) that which is composed predominantly of the |3141 1〉, |2142 251 -1〉 and |2142 051 1〉 states. Pulses of tunable IR excited molecules to the lower component (II) of one of the Fermi dyads and the evolution of population in the upper component (I) was observed by exciting laser-induced fluorescence (LIF) from this level using tunable UV laser radiationIn this Letter, we employ the notation for vibrational states whereby, for example, 31 denotes one quantum of excitation in the ν3 normal mode. (31/214151)I, II denotes the Fermi dyad in which the principal contributions to the vibrational eigenstates are from the normal mode wavefunctions describing the zeroth-order 31 fundamental and 214151 combination vibrational states. In each dyad, the subscript II is used to denote the lower of the two component states, I the higher. Analysis of the LIF signals vs. time yields the following rate coefficients (kid) for intradyad transfer at 295 K: for (31/214151)I↔II, kid=(2.1±0.2)×10-10 cm3 molecule-1 s-1; for (3141/214251)I↔II, kid=(3.2±0.6)×10-11 cm3 molecule-1 s-1. These results are discussed in terms of the matrix elements for such collision-induced transitions and differences in the mixing of the zero-order states in these two pairs of Fermi dyads.

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