Infrared emission from the reaction of CHF ((X)over-tilde-(1)A') with NO

Infrared emission has been observed from the reaction of the CHF (X̃1A′) radical with NO (X2Π). The carbene radical was formed by infrared multiphoton dissociation (IRMPD) of either the CH2FCl or the CH2F2 precursor, and emission in the 1850-4500-cm-1 region was observed by a time-resolved Fourier t...

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Main Authors: Brownsword, R, Hancock, G, Oum, K
Format: Journal article
Language:English
Published: 1996
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author Brownsword, R
Hancock, G
Oum, K
author_facet Brownsword, R
Hancock, G
Oum, K
author_sort Brownsword, R
collection OXFORD
description Infrared emission has been observed from the reaction of the CHF (X̃1A′) radical with NO (X2Π). The carbene radical was formed by infrared multiphoton dissociation (IRMPD) of either the CH2FCl or the CH2F2 precursor, and emission in the 1850-4500-cm-1 region was observed by a time-resolved Fourier transform infrared (FTIR) technique. Emissions have been identified from the HF product of the reaction and from species produced by the subsequent reaction of the NCO radical product with NO. The HF was found to possess more than a statistical share of the available energy in vibration. Addition of D2 to the system results in DF formed from the reaction of F atoms, and comparison of the HF/DF emission intensities has allowed the relative branching ratio of the CHF + NO reaction forming HF and F products to be 0.6 ± 0.04:0.4 ± 0.03. © 1996 American Chemical Society.
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spelling oxford-uuid:c4c1a80b-ea3f-48d8-b005-a760c70d04642022-03-27T06:25:55ZInfrared emission from the reaction of CHF ((X)over-tilde-(1)A') with NOJournal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:c4c1a80b-ea3f-48d8-b005-a760c70d0464EnglishSymplectic Elements at Oxford1996Brownsword, RHancock, GOum, KInfrared emission has been observed from the reaction of the CHF (X̃1A′) radical with NO (X2Π). The carbene radical was formed by infrared multiphoton dissociation (IRMPD) of either the CH2FCl or the CH2F2 precursor, and emission in the 1850-4500-cm-1 region was observed by a time-resolved Fourier transform infrared (FTIR) technique. Emissions have been identified from the HF product of the reaction and from species produced by the subsequent reaction of the NCO radical product with NO. The HF was found to possess more than a statistical share of the available energy in vibration. Addition of D2 to the system results in DF formed from the reaction of F atoms, and comparison of the HF/DF emission intensities has allowed the relative branching ratio of the CHF + NO reaction forming HF and F products to be 0.6 ± 0.04:0.4 ± 0.03. © 1996 American Chemical Society.
spellingShingle Brownsword, R
Hancock, G
Oum, K
Infrared emission from the reaction of CHF ((X)over-tilde-(1)A') with NO
title Infrared emission from the reaction of CHF ((X)over-tilde-(1)A') with NO
title_full Infrared emission from the reaction of CHF ((X)over-tilde-(1)A') with NO
title_fullStr Infrared emission from the reaction of CHF ((X)over-tilde-(1)A') with NO
title_full_unstemmed Infrared emission from the reaction of CHF ((X)over-tilde-(1)A') with NO
title_short Infrared emission from the reaction of CHF ((X)over-tilde-(1)A') with NO
title_sort infrared emission from the reaction of chf x over tilde 1 a with no
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AT hancockg infraredemissionfromthereactionofchfxovertilde1awithno
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