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HERO ID
5963107
Reference Type
Journal Article
Title
A REGIOSPECIFIC CYCLOADDITION - SUCCESSIVE REACTIONS OF .CH(2)CH(2)OH()+ WITH CH(2)O
Author(s)
Mourgues, P; Audier, HE; Hammerum, S
Year
1994
Is Peer Reviewed?
1
Journal
Rapid Communications in Mass Spectrometry
ISSN:
0951-4198
EISSN:
1097-0231
Volume
8
Issue
1
Page Numbers
53-55
DOI
10.1002/rcm.1290080110
Web of Science Id
WOS:A1994MT55300009
URL
http://doi.wiley.com/10.1002/rcm.1290080110
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Abstract
Four dominant reactions can be observed when the beta-distonic ion .CH2CH2OH2+ reacts in the cell of a Fourier-transform ion cyclotron resonance spectrometer with a number of neutral molecules: protonation of the neutral molecule, ethylene radical-cation transfer, hydride abstraction from the neutral molecule, and charge exchange. Among the ethylene transfer reactions, which can lead to a variety of other distonic ions, we have throroughly studied the reaction with formaldehyde. The reaction of a first molecule of CH2O yields .CH2CH2OCH2+. The addition of a second one leads to 1,3-dioxane which stabilizes by H. loss. This latter reaction is regiospecific.<
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OPPT REs
•
OPPT_1,4-Dioxane_D. Exposure
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