## 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
Mass spectrometry—III: Further studies of the unimolecular decomposition of acetophenone azine in the gas phase induced by electron-impact
✍ Scribed by Stuart E. Scheppele; Ronald D. Grigsby; Donald W. Whitaker; Susan D. Hinds; Keith F. Kinneberg; Ronald K. Mitchum
- Publisher
- John Wiley and Sons
- Year
- 1970
- Tongue
- English
- Weight
- 590 KB
- Volume
- 3
- Category
- Article
- ISSN
- 1076-5174
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✦ Synopsis
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 formed via loss of ring hydrogen. Within experimental uncertainty the major fragmentation reactions of the molecular ion of I, the [M –1] ion, and the [M –15] ion occur without loss of structural identity of the phenyl and methyl moieties. Ionization of I occurs with a high degree of structural integrity.
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