Abstract
Mono-, di- and trichlorophenyl (4-pyridyl) ketones and a selection of their 3-pyridyl isomers follow similar mass spectral fragmentation paths. In the case of the phenyl (4-pyridyl) ketones the major primary fragmentation reaction of the intense molecular ion is the loss of the pyridyl group, while the corresponding 3-pyridyl ketones decay primarily by cleavage of the aryl—Cl bond or the aryl—CO bond.
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Herzig, U., Varmuza, K. & Krenmayr, P. Synthese und massenspektrometrische Untersuchungen von Phenyl-pyridyl-ketonen. Monatshefte für Chemie 108, 191–197 (1977). https://doi.org/10.1007/BF00900922
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DOI: https://doi.org/10.1007/BF00900922