A stable ethanal...H+...ethanol proton-bridged dimer (2) by decomposition of CH,CH(OC,H,)CH(OC,H,)CH~ ' was formed in the ion source of a Fourier transform ion cyclotron resonance (FT-ICR) mass spectrometer and also in the second field-free region of a reverse-geometry mass spectrometer. Its structu
Secondary isotope effects in the mass spectra of C2D5OC2H5 and CD3CH2OC2H5
β Scribed by Morley E. Russell
- Publisher
- John Wiley and Sons
- Year
- 1993
- Tongue
- English
- Weight
- 248 KB
- Volume
- 28
- Category
- Article
- ISSN
- 1076-5174
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β¦ Synopsis
Secondary isotope effects were examined in the loss of methyl from the molecular ions of C,D,OC,H, and CD,CH,OC,H, for ion source processes and collisional activation (CA) processes. In the ion source loss of CH, was slightly favored over loss of CD, , but in CA the CH, loss was favored to a much larger extent than expected. A possible explanation is given which invokes an energy distribution function peaked near the appearance energy for the methyl loss process.
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