## Abstract A collision‐induced dissociation (CID) study of five synthesized nitramines was carried out using a hybrid EBQQ mass spectrometer. CID spectra were obtained in two modes: __B/E__ linked‐scan mode and MS/MS mode using the EB sector combination as the first mass spectrometer and the QQ as
Mass spectral fragmentation pathways in some glycoluril-type explosives. A study by collision-induced dissociation and isotope labeling
✍ Scribed by J. Yinon; S. Bulusu; T. Axenrod; H. Yazdekhasti
- Publisher
- John Wiley and Sons
- Year
- 1994
- Tongue
- English
- Weight
- 435 KB
- Volume
- 29
- Category
- Article
- ISSN
- 1076-5174
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✦ Synopsis
Abstract
Electron impact (EI), chemical ionization and negative‐ion chemical ionization (NCI) mass spectra of 1,4‐dinitroglycoluril (DINGU), its ^15^N‐ and ^2^H‐labeled analogues and the dimethyl‐substituted derivatives were recorded. Tandem mass spectrometry with collision induced dissociation was used to study the fragmentation pathways of these compounds. It was found that the main EI fragmentation processes of DINGU are due to the cleavage of CN bonds and some rearrangement reactions.
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A collipiobiaduced dissociation study of a series of dinitrmromatic compounds was carried out using a tandem BB mpss spectrometer. Fra.gmentation pathways were determid in the electron impact mode. Loss of NO,' from the molecular ion was observed in most of tbe investigated compouods. In some compau
## Abstract A collision‐induced dissociation (CID) study of a series of aminonitrobenzenes was carried out using a tandem __BB__ mass spectrometer. Fragmentation pathways were determined in the electron impact mode. Loss of NO^·^ was found to be a major decomposition process. Peaks formed by this p