The 70 eV electron impact mass spectra of some para-substituted N-heteroaryl benzylamines, synthesized through the corresponding Schiff bases, are reported. Typical fragmentation patterns are discussed with the aid of mass analyzed ion kinetic energy spectra and exact mass measurements. The compounds are relatively stable under electron impact, the molecular ion being the base peak or the second most intense ion in the spectra. The dominating breakdown process is the benzylic cleavage, that gives rise to the base peak in some of the investigated compounds and to the second intense peak in others.
|Titolo:||ELECTRON-IMPACT MASS-SPECTRA OF PARASUBSTITUTED N-HETEROARYL BENZYLAMINES|
|Data di pubblicazione:||1994|
|Appare nelle tipologie:||1.1 Articolo in rivista|