Abstract

Amino acid derived oxovanadium Schiff base complexes and their in situ (oxo)-peroxovanadium Schiff base complexes were first studied with electrospray ionization tandem mass spectrometry (ESI-MS n) with collision-induced dissociation (CID). Their fragmentation pathways are proposed on the base of the MS n studies. All of the molecular ions of the two group vanadium complexes easily lose a CO 2 molecule under ESI-MS condition. In the dissociation, H 2O, VO 2 will possibly be eliminated for oxovanadium Schiff base complexes, while (oxo)-peroxovanadium Schiff base complexes always yield the same ion at m/ z 314 due to elimination of a molecule of aldehyde from amino acid residues. The dissociation rules may be extended to other metal Schiff base complexes and other peroxo-metal complexes.

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