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Investigation of the ionization processes occurring in liquid‐assisted secondary ion mass spectrometry of derivatized monosaccharides
Author(s) -
Paul G. J. C.,
Théberge R.,
Bertrand M. J.,
Feng R.,
Bailey M. D.
Publication year - 1993
Publication title -
organic mass spectrometry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.475
H-Index - 121
eISSN - 1096-9888
pISSN - 0030-493X
DOI - 10.1002/oms.1210281108
Subject(s) - chemistry , electrospray ionization , mass spectrometry , secondary ion mass spectrometry , monosaccharide , analytical chemistry (journal) , ionization , ion , solvation , mass spectrum , protonation , organic chemistry , chromatography
Several derivatized monosaccharides, the 2‐deoxy‐ D ‐ribofuranoses, have been studied by liquid‐assisted secondary ion mass spectrometry (LSIMS) in order to gain insight into the factors affecting ionization in FAB/LSIMS. Examination of the mass spectra for these compounds obtained in eight liquid matrices (diethanolamine, ethylene glycol, glycerol, 2‐hydroxyethyl disulfide, 2‐hydroxyphenethyl alcohol, 3‐nitrobenzyl alcohol, sulfolane and thioglycerol) reveals that in all cases the anomalous [M – H] + ion is the predominant species in the molecular ion region and that [M + Na] + species are observed in the presence of Na + . The analysis of these compounds by chemical ionization with ammonia shows [M + H] + as the major species while [M – H] + is essentially absent. This indicates that the ionization processes occurring in the two techniques are not analogous. Thermodynamic considerations based on the gas‐phase hydride ion affinities of the protonated matrices do not support a predominant gas‐phase mechanism for the formation of [M – H] + in LSIMS. However, it is possible using solvation energies to rationalize the formation of [M – H] + in terms of condensed‐phase ionization processes which take place either in the liquid matrix or in the dense selvedge region immediately above the surface where extensive solvation is present. Electrospray data obtained for one of the derivatized monosaccharides indicates that the [M – H] + is not performed in the condensed phase in LSIMS and that it is the product of fast ion beam‐induced processes. While the nature of the matrix is seen to have little effect on the intensities of [M – H] + and [M + H] + it is observed to be an important factor for the intensity of M + ˙ for one of the monosaccharides. This effect can be related to the electron‐scavenging properties of the matrices and reinforces the hypothesis that condensed phase processes are significant in ionization.