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Structural „memory effects”︁ influencing decompositions of glucose alkoxide anions produced from monoterpene glycoside isomers in tandem mass spectrometry
Author(s) -
Cole R. B.,
Tabet J. C.,
Salles C.,
Jallageas J. C.,
Crouzet J.
Publication year - 1989
Publication title -
rapid communications in mass spectrometry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.528
H-Index - 136
eISSN - 1097-0231
pISSN - 0951-4198
DOI - 10.1002/rcm.1290030302
Subject(s) - chemistry , tandem mass spectrometry , mass spectrometry , alkoxide , decomposition , ion , monoterpene , tandem , chromatography , organic chemistry , catalysis , materials science , composite material
Isomeric glycoconjugates have been distinguished using desorption negative‐ion chemical ionization/tandem mass spectrometry (DNCI–MS/MS). The structure of the leaving terpene influences the orientation of consecutive decompositions during collisionally activated decomposition (CAD) of [M–H] − ions which pass through a glucose alkoxide intermediate ion. This apparent „memory effect” can be rationalized by considering the production of anion‐induced dipole complexes.

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