The structure and mechanism of formation of C5H9O+ from ionized phytyl methyl ether
Author:
Affiliation:
1. Chemistry and Chemical Technology, University of Bradford, BD7 1DP, Bradford, West Yorkshire, England
2. Department of Chemistry, University of Warwick, CV4 7AL, Coventry, England
3. , 650 North Tippecanoe Street, 46403, Gary, Indiana, USA
Publisher
American Chemical Society (ACS)
Subject
Spectroscopy,Structural Biology
Link
https://pubs.acs.org/doi/pdf/10.1016/1044-0305%2895%2900679-6
Reference26 articles.
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3. Distonic radical cations in gaseous and condensed phase
4. Gas phase analogues of solvolysis reactions
5. On the structure of the C2H4O2 neutrals (acetic acid versus 1,1-dihydroxyethene) generated from ionized n-hexanoic acid and n-butyl acetate in the gas phase. Implications for the mechanism of the McLafferty rearrangement
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1. Differentiation of isomeric allylic alkenyl methyl ethers by Raman spectroscopy;Analytica Chimica Acta;2007-08
2. Reactions of low-energy pentenyl methyl ether radical cations C2H5CHCHCH2OCH3+, CH2CHCH(C2H5)OCH3+ and CH2C(C2H5)CH2OCH3+;International Journal of Mass Spectrometry;2002-06
3. Reactions of ionised methyl pent-4-enyl ether, CH2CH(CH2)3OCH3·+;International Journal of Mass Spectrometry;2001-09
4. Dissociation Reactions of Low-Energy Pentenyl Methyl Ether Radical Cations C5H9OCH3•+;European Journal of Mass Spectrometry;2001-06
5. Reactions of metastable ionized γ, γ-dialkylallyl methyl ethers: relative rates for elimination of alkyl radicals by formal γ-cleavage;International Journal of Mass Spectrometry and Ion Processes;1997-11
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