Hydrogenation of quinone compounds during secondary ion mass spectra measurement.
- 1 January 1989
- journal article
- research article
- Published by Japan Antibiotics Research Association in The Journal of Antibiotics
- Vol. 42 (1) , 49-53
- https://doi.org/10.7164/antibiotics.42.49
Abstract
Antibiotics containing a quinone group show characteristic reduced pseudo-molecular ions (M+2)+ and (M+3)+ during the measurements of secondary ion mass spectra using glycerol as a matrix. The ratios of peak intensities (M+2)+ and (M+3)+ over (M+1)+ increase with time. As this phenomenon is not found using sulfolane as a matrix, the quinone group seems to be hydrogenated to a hydroquinone by active hydrogen which is produced from a free hydroxyl group of the glycerol by bombardment with the Xe+ beam. This hydrogenation reaction is specific for the quinone group.This publication has 3 references indexed in Scilit:
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- Structure and conformation of saframycin R determined by high field 1H and 13C NMR and its interactions with DNA in solution.The Journal of Antibiotics, 1983
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