## Abstract Mass spectra of acetophenone azine‐d~10~ (II) and acetophenone azine‐d~6~ (III) were obtained to ascertain the validity of the proposed mass spectral fragmentation mechanisms proposed for acetophenone azine (I). Data from II and III reveal that the [M –1] ion in the spectrum of I is for
Mass spectrometry—II: The unimolecular decomposition of benzaldehyde azine in the gas phase induced by electron-impact
✍ Scribed by Stuart E. Scheppele; Ronald D. Grigsby; Keith F. Kinneberg; Earl D. Mitchell; Claude A. Mannan
- Publisher
- John Wiley and Sons
- Year
- 1970
- Tongue
- English
- Weight
- 745 KB
- Volume
- 3
- Category
- Article
- ISSN
- 1076-5174
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✦ Synopsis
Abstract
The mass spectra of benzaldehyde azine‐α, αA‐d^2^ (III) and benzaldehyde azine‐d^10^ (IV) reveal that both ring and α hydrogen are lost from the molecular ion of benzaldehyde azine (II) in forming the [M –1] ion. Data from the spectra of III and IV at 70 eV and reduced ionizing voltages are consistent with the existence of two competing pathways producing [M –1] ions. Rearrangement ions are observed in the spectra of II. Randomization is unimportant in the electron‐impact‐induced fragmentation reactions of II. The rearrangement‐fragmentation reactions for II in general parallel those previously observed for acetophenone azine (I).
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