Negative chemical ionization mass spectrometry of explosives
โ Scribed by Willem J. Bouma; Keith R. Jennings
- Publisher
- John Wiley and Sons
- Year
- 1981
- Tongue
- English
- Weight
- 444 KB
- Volume
- 16
- Category
- Article
- ISSN
- 1076-5174
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โฆ Synopsis
Abstract
The negative chemical ionization mass spectra of nitrobenzene, ethylene glycol dinitrate and nitroglycerine have been obtained using various reagent ions. For nitrobenzene, [OH]^โ^ gives the [M โ H]^โ^, together with [M]^โห^ ions formed by electron capture, but other reagent ions gave relatively low intensity adduct peaks. Ethylene glycol dinitrate and nitroglycerine gave abundant [M + X]^โ^ ions (X = NO~2~, NO~3~, Cl, Br, I), together with ions arising from the thermal decomposition of the samples in the heated inlet system. The rate of anion attachment to these compounds is much greater than that to related compounds having only one functional group, and it is suggested that this is due to the participation of the adjacent groups in the bonding between the substrate and anion.
๐ SIMILAR VOLUMES
In order to utilize the selectivity of negative chemical ionization mass spectrometry for amine analysis we have examined a number of biogenic amine derivatives for detection limits, molecularly specific characterization and ease of preparation using negative chemical ionization mass spectrometry wi
Gas chromatography-negative chemical ionization mass spectrometry (GC-NCIMS) has been applied to the analysis of 0-and S-glucuronides. The glucuronides were derivatized with pentafluorobenzyl (PFB) bromide and Tri-Sil, and analyzed by GC-NCIMS. All glucuronides gave a large [M-PFBI-ion indicative of