The unimolecular fragmentation reactions of 28 protonated nitroarenes, occurring on the metastable ion time-scale, are reported. In addition, the collision-induced fragmentation of the same species have been studied at 10 eV and at 50 eV collision energy. When an OH, COOH or NH, substituent is ortho to the nitro function, the dominant fragmentation involves loss of H,O, for both unimolecular and collision-induced reactions. When there is an electron-releasing substituent ortho or para to the nitro group, loss of OH is the dominant fragmentation reaction both on the metastable ion time-scale and for ions activated by collision. When the electron-releasing substituent is meta to the nitro group, loss of NO, is the dominant low-energy unimolecular fragmentation reaction while loss of HNO, is the most important fragmentation for ions activated by 50 eV collisions. Elimination of NO from [MH]+ occurs to a significant extent in the unimolecular fragmentation of protonated nitrobenzene and those protonated nitrobenzenes containing electron-attracting substituents. In the collision-induced dissociation of these species loss of HNO, occurs at the expense of loss of NO. The results are consistent with protonation predominantly at the nitro group. The results are discussed in terms of the use of neutral loss scans in tandem mass spectrometry to monitor complex mixtures for nitroarenes. The authors are indebted to the Natural Sciences and Engineering Research Council for financial support. A.G.H. gratefully acknowledges the award of a Killam Research Fellowshiu (1985-87) bv the . .
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However, in even more cases, such as the nitrotoluenes, Canada Council.