Nucleophilic attack by the acetonyl anion (CH3COCH 2-) on highly electron-deficient nitroaromatics such as trinitrotoluene (TNT) results in the carbon-bonded anionic σ-complexes (Meisenheimer complexes). The complexes are generated at atmospheric pressure with relatively low internal energy and do not dissociate under atmospheric pressure chemical ionization conditions, but can be dissociated upon collisional activation to produce characteristic nitrobenzyl-substituted acetonyl anions via elimination of HNO2. Further fragmentation produces deprotonated nitrotoluene anions through the loss of CH2CO, while loss of CH 2COCH3 and CH3COCH3 yields nitroaromatic molecular anions and their H-loss counterparts. Hydrogen/deuterium (H/D) scrambling is observed in the fragmentation products of the [TNT·CD3COCD2]- complex to extents which vary for different fragmentation pathways. Selective Meisenheimer complex formation, together with its distinctive fragmentation pattern, supplies a highly discriminatory method for detection of TNT and related compounds.
|Original language||English (US)|
|Number of pages||7|
|Journal||Rapid Communications in Mass Spectrometry|
|State||Published - Dec 5 2005|
All Science Journal Classification (ASJC) codes
- Analytical Chemistry
- Organic Chemistry