Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/23520
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Type: Journal article
Title: The formation of the stable radicals •CH₂CN, CH₃•CHCN and •CH₂CH₂CN from the anions ⁻CH₂CN, CH₃⁻CHCN and ⁻CH₂CH₂CN in the gas phase. A joint experimental and theoretical study
Other Titles: The formation of the stable radicals (.)CH(2)CN, CH(3)(.)CHCN and (.)CH(2)CH(2)CN from the anions (-)CH(2)CN, CH(3)(-)CHCN and (-)CH(2)CH(2)CN in the gas phase. A joint experimental and theoretical study
Author: Andreazza, H.
Fitzgerald, M.
Bowie, J.
Citation: Organic and Biomolecular Chemistry, 2006; 4(12):2466-2472
Publisher: Royal Soc Chemistry
Issue Date: 2006
ISSN: 1477-0520
1477-0539
Statement of
Responsibility: 
Hayley J. Andreazza, Mark Fitzgerald and John H. Bowie
Abstract: Franck–Condon one-electron oxidation of the stable anions ⁻CH₂CN, CH₃⁻CHCN and ⁻CH₂CH₂CN (in the collision cell of a reverse-sector mass spectrometer) produce the radicals •CH₂CN, CH₃•CHCN and •CH₂CH₂CN, which neither rearrange nor decompose during the microsecond duration of the neutralisation–reionisation experiment. Acetonitrile (CH₃CN) and propionitrile (CH₃CH₂CN) are known interstellar molecules and radical abstraction of these could produce energised •CH₂CN and CH₃•CHCN, which might react with NH₂• (a known interstellar radical) on interstellar dust or ice surfaces to form NH₂CH₂CN and NH₂CH(CH₃)CN, precursors of the amino acids glycine and alanine.
Keywords: Free Radicals
Gases
Nitriles
Acetonitriles
Molecular Conformation
Thermodynamics
Mass Spectrometry
Description: Copyright © Royal Society of Chemistry 2006 Reproduced by permission of The Royal Society of Chemistry
DOI: 10.1039/b602621d
Published version: http://dx.doi.org/10.1039/b602621d
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Chemistry publications

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