## 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
Mass spectral fragmentation pathways in nitramines. A collision-induced dissociation study
✍ Scribed by Jehuda Yinon; William C. Brumley; George M. Brilis; Suryanarayana Bulusu
- Publisher
- John Wiley and Sons
- Year
- 1990
- Tongue
- English
- Weight
- 325 KB
- Volume
- 25
- Category
- Article
- ISSN
- 1076-5174
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✦ Synopsis
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 collision cell and second mass spectrometer, respectively. Fragmentation pathways of the compounds were determined in the electron‐impact mode. It was found that dominant fragmentation pathways included the loss of OH, NO~2~ and HNO~2~ in addition to the loss of CH~2~NNO and CH~2~NNO~2~.
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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 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