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  • 1
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 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.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Rapid Communications in Mass Spectrometry 6 (1992), S. 485-491 
    ISSN: 0951-4198
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Physics
    Notes: An Approach which allows the determination of the specific effects of experimental parameters on the extent of reduction observed in fast-atom bombardment/liquid-assisted secondary-ion mass spectrometry (FAB/LSIMS) has been developed. The methodology is based on the isolation of the different components-background, reduction extent, and isotopic abundances - which contribute to peak intensities in the molecular-ion cluster. The individual contributions of reduction and background are calculated by an algorithm SRBC (simulated reduction and background calculations) which utilizes a Monte-Carlo method to optimize the values obtained for these variables. This approach has been used to examine the effects of analyte concentration, primary-beam energy and beam density on the extent of reduction in FAB/SIMS experiments. The results obtained indicate that the beam energy has no significant effect on the apparent reduction, as measured by the experimental (A+2)/A isotope peak ratio, while analyte concentration and beam density effects are obseerved. However, background and reduction data generated by SRBC demonstrate that in some cases there is little effect of these parameters on the true reduction of the analyte and that the increase in apparent reduction with the variation in these parameters results mainly from an artefact created by an increase in the background signal at lower concentrations and higher beam densities.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The effect of experimental parameters such as time of irradiation, analyte concentration, primary beam density, matrix selection and matrix additives on the beam-induced dehalogenation of chlorpromazine in liquid secondary ion mass spectrometry (LSIMS) was investigated. It was found that dehalogenation of chlorpromazine in glycerol increased with increasing time of irradiation, analyte concentration and primary beam density. These results were compared with those obtained using 4-chlorophenylalanine ethyl ester and the differences observed were rationalized in terms of compound surface activity. Evidence is given that matrix selection is the key experimental parameter affecting the extent of beam-induced dehalogenation of chlorpromazine in LSIMS. Of the eleven matrices used, the greatest extent of dehalogenation was observed in glycerol. Sulfur-containing matrices consistently exhibited a lower extent of dehalogenation than oxygen-containing aliphatic matrices, implying that sulfur is implicated in mitigating the reduction process. Dehalogenation was totally inhibited in 2-hydroxyethyl disulfide, 4-hydroxybenzenesulfonic acid and 3-nitrobenzyl alcohol. Similarly, the use of matrix additives such as 3-nitrobenzyl alcohol and trifluoroacetic acid was found to be useful in inhibiting the extent of dehalogenation occurring in glycerol.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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