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MASS-SPECTRAL FRAGMENTATION PATHWAYS IN SOME GLYCOLURIL-TYPE EXPLOSIVES - A STUDY BY COLLISION-INDUCED DISSOCIATION AND ISOTOPE LABELING
Journal article   Peer reviewed

MASS-SPECTRAL FRAGMENTATION PATHWAYS IN SOME GLYCOLURIL-TYPE EXPLOSIVES - A STUDY BY COLLISION-INDUCED DISSOCIATION AND ISOTOPE LABELING

J YINON, S BULUSU, T AXENROD and H YAZDEKHASTI
Organic Mass Spectrometry, Vol.29(11), pp.625-631
Nov/1994
url
https://doi.org/10.1002/oms.1210291109View
Published (Version of record) Restricted
url
https://ezproxy.weizmann.ac.il/login?url=http://dx.doi.org/10.1002/oms.1210291109View
Published (Version of record) Restricted

Abstract

Electron impact (EI), chemical ionization and negative-ion chemical ionization (NCI) mass spectra of 1,4-dinitroglycoluril (DINGU), its N-15- and H-2-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 C-N bonds and some rearrangement reactions.

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