The ion-molecule reactions between protonated acetaldehyde and methanol were explored on a quadrupole, quistor, quadrupole tandem mass spectrometer. In addition to proton transfer to methanol and subsequent methanol ionmolecule chemistry, the protonated acetaldehyde-methanol adduct and methylated ac
Hydroxylation of selected hydrocarbon ions on reaction with methanol in the gas phase
✍ Scribed by Gregory G. Dolnikowski; John Allison; J. Throck Watson
- Publisher
- John Wiley and Sons
- Year
- 1990
- Tongue
- English
- Weight
- 509 KB
- Volume
- 25
- Category
- Article
- ISSN
- 1076-5174
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✦ Synopsis
The ion-molecule reactions of selected hydrocarbon cations with methanol which lead to the production of hydroxylated odd-electron molecular ions in the high-pressure ion source of a mass spectrometer or in the central quadrupole of a tandem quadrupole mass spectrometer are described. A wide variety of hydrocarbon cations were investigated, including aliphatic and aromatic cations; of these, only those having a vacant site on an aromatic system appear to undergo the bydroxylation reaction in high yield. A mechanism is proposed for the formation of the molecular ion of phenol from the ion-molecule reaction involving the phenyl cation with methanol. In addition, thermochemical data are provided which support the formation of the postulated species.
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