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  • Analytical Chemistry and Spectroscopy  (9)
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  • Analytical Chemistry and Spectroscopy  (9)
  • Chemistry  (9)
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  • 1
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 12 (1977), S. 28-32 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: In the field desorption mass spectrometry of oligosaccharides, traces of contaminating salts in polar solvents decrease the detection sensitivity, and in some cases no ion could be detected in the molecular range. The present work shows that the addition of alkaline salts (NaI or KI) greatly increases the sensitivity, and cationized molecular ions are obtained. The influence of the molar ratio sugar/salt on the nature and relative intensity of the desorbed species has been studied on mixtures of α-D-trehalose and NaI. At the low salt ratio (100:1), high molecular weight clusters [XM + Na]+ are preferentially formed. At the high salt ratio (1:10), mixed clusters [M + NaI + Na]+, doubly charged ions [M + 2Na]2+ and monomeric cationized ions [M + Na]+ are observed along with salt clusters [NaI + Na]+ and [2NaI + Na]+. In the range of molar ratios sugar/salt of 10:1 to 1:1, the field desorption mass spectra exhibit a cationized ion [M + Na]+, which contributes more than 80% of Σ100. This cationization technique has been applied to the field desorption mass spectrometry of several oligosaccharides. In all cases, the salt effect causes the replacement of the [M + H]+ ion by a [M + C]+ ion. (Note: the term [M + C]+ and similar ones mean an association between the whole molecule studied (M) and an alkaline cation [C]+ ([K)]+, [Na]+, [Li]+).) Thus, di, tri- and tetrasaccharides exhibit intense [M + Na]+ ions in the presence of NaI and only a few fragment peaks are observed in their field desorption mass spectra. This technique has been applied successfully to the detection of the hexasaccharide ajugose in a natural sample of pentasaccharide, and has also allowed the unambiguous determination of the composition of a mixture of partially methylated trehaloses. The salt effects are dicussed in terms of selective adsorption on the emitter, pre-existing soluble complexes sugar-salt, interactions between these species in the electric field and dissociative desorption of ionic complexes.
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  • 2
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Electron impact mass spectrometry of an imido-sulfite 5,6-benzo-2-imino-N-(2,4,6-trichlorophenyl)-1,3-dioxa-2-thiacycloheptane shows an intense fragment ion corresponding to the expulsion of SO2H from the molecular ion. A mechanism that requires a rearrangement of the molecular ion is proposed. Structural elucidation of the [M—SO2H]+ ion was obtained by recording its metastable ion and collisional activation spectra. Comparison of these spectra with similar spectra recorded from a precursor ion of known structure demonstrated that they were identical. Thus, the results support the proposed structure which derives from the expulsion of SO2H from the molecular ion of the compound 5,6-benzo-2-imino-N-(2,4,6-trichlorophenyl)-1,3-dioxa-2-thiacycloheptane.
    Additional Material: 4 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 20 (1985), S. 525-529 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The distinction between 17-epimeric 3,17-dioxygenated hydroxyandrostanes has been made by comparison of both their methane or ammonia positive and OH- negative chemical ionization (CI) mass spectra. In the methane or ammonia positive CI, the 17α-configuration in the eight stereoisomeric 5ξ-androstane-3ξ,17ξ-diols can be determined by the relative abundances of the ion [MH—2 H2O]+. In the ammonia CI spectra, the ion [M+NH4—H2O]+ possesses only a low abundance, but a comparison of the relative rates of the loss of water v. the loss of ammonia from [M.NH4]+ in the second field-free region allows a clear distinction to be made between the 17α- and 17β-series. In the OH- negative CI mass spectra, the 5ξ-androstane-3-one-17ξ-ols produce an intense ion [M—H—H2O]- in the 17α-series only.
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  • 4
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 19 (1984), S. 448-451 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: FAB positive mass spectra of trehalose in the presence of different matrices such as glycerol, diethanolamine (DEA) and triethanolamine (TEA) are presented and discussed. Protonated and solvated protonated trehalose ions are observed, of which the relative abundance changes with the liquid matrix used. MIKE spectra of the protonated molecular ions solvated by the matrix show unambiguously that desolvation contributes to the formation of protonated molecular ions. It is shown that the decomposition of these complexes is mainly controlled by the relative proton affinities of the analysed sample and the matrix.
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  • 5
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 22 (1987), S. 6-12 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The oxyanion [M—H]- from several methylglycosides were generated by fast atom bombardment and their decomposition was studied by mass-analysed ion kinetic energy spectrometry. The main decomposition pathway is the loss of methanol. The hydroxylic hydrogen arises by proton transfer from the hydroxyl groups of the sugar. In the gluco-series, no anomeric effect is found. The absence of either the hydroxyl groups at C-2 or C-6 does not inhibit the glycosidic cleavage. However, the blocking of both the hydroxyl groups at C-4 and C-6, by a benzylidene group or two methyl groups, inhibit completely the glycosidic cleavage. From these results, it is proposed that the glycosidic cleavage occurs after opening the sugar ring by a vicinal attack of an oxyanion at C-6 or C-4 to the C-5 carbon atom. Then, the ionized hemi-acetals fragment into a methanolate anion and a 5,6- or 4,5-anhydrosugar which exchange another proton before their separation into charged and neutral species.
    Additional Material: 4 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 28 (1993), S. 455-458 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Silver ion adducts of several methyl glycopyranosides were generated by fast atom bombardment of 1:1 mixtures of the glycosides with silver nitrate. The unimolecular decompositions of [M + Ag]+ ions showed dramatic differences related to the relative positions of both the hydroxyl group on C(2) and the anomeric methoxyl group. When these groups were in the cis position, methanol was exclusively expelled. When they were in the trans position, silver hydride was preferentially lost. The stereoselective elimination reaction is proposed to proceed through a five-membered silver-containing intermediate complex, from the oxygen on C(2) to the anomeric substituent (methoxyl group or hydrogen atom).
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  • 7
    ISSN: 1052-9306
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Mass spectrometry has been used for testing the chemical purity of some new antitumor cyclophosphazene compounds. The spectrum of N3P3Az6 (code name MYKO 63) - which exhibits noticeable activity on murine P 388, L 1210 and B 16 tumors - appeared to be remarkably simple, as most of the fragmentations arose from successive losses of the aziridino radicals. Traces of the pentaziridinomonochloro impurity formed by an incomplete substitution of N3P3Cl6 chlorine atoms under aziridinolysis could be detected in an impure and toxic sample by spectral subtraction. Quantification of this impurity was performed by selected ion monitoring in the direct inlet mode of sample introduction. The mass spectra of other derivatives of this class of compounds are slightly more complex, since the decomposition pathways showed more intense H-transfers associated with the loss of substituents.
    Additional Material: 10 Ill.
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  • 8
    ISSN: 1052-9306
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The fatty acyl moiety in lanosterol and dihydrolanosterol esters was determined by measurement of the metastable transition [M - 15]+ → [M - 15-fatty acid]+ which occurs in the first field free region of a double focusing mass spectrometer. The analysis was made by accelerating voltage scanning. Quantification of the esters was made by single reaction monitoring, using calibration curves measured in the presence of the corresponding matrix. The detection limit for a selected lanosterol ester was below 300 pg. Using this technique, each individual lanosterol and dihydrolanosterol ester was detected and quantified in a sample of wool wax. Interference from dihydroagnosterol esters is very likely, but interference from sterol esters which do not have a 4-methyl group is unlikely since the corresponding metastable peak is of very low intensity.
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  • 9
    ISSN: 1052-9306
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The characterization of two abnormal human haemoglobins by fast atom bombardment (FAB) mapping is presented. The first variant, called ‘R’, exhibits a tryptic FAB map identical to that of normal haemoglobin. However, using Staphylococcus protease V8, a peptide containing the carboxyl end of the β-chain exhibits a mass shift down to 300 mass units. This clearly indicates the deletion of the two last amino acids of the β-chain. The second variant, called ‘Grenoble’, is due to two different modifications of the β-chain. The location of the Pro → Ser exchange on peptide T5 is achieved by the collisionally activated dissociation mass analyzed ion kinetic energy spectra of the corresponding [MH]+ ion. The m/z value of that peptide indicated a supplementary acid → amide modification, which was located by amino acid sequencing using chemical methods. This work concludes with the necessity of using complementary methods for achieving rapid determinations of abnormal proteins with minute amounts.
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