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  • Analytical Chemistry and Spectroscopy  (2)
  • 1985-1989  (2)
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Keywords
  • Analytical Chemistry and Spectroscopy  (2)
  • Chemistry  (2)
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Year
  • 1
    ISSN: 0887-6134
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A capillary supercritical fluid chromatography/mass spectrometry interface incorporating a heated frit restrictor is described. The trichothecene mycotoxins T-2 toxin, deoxynivalenol and roridin A were used to evaluate the effect of restrictor temperature and carbon dioxide mobile phase on the negative ion chemical ionization (CI) spectra of these compounds under electron capture, proton abstraction and chloride attachment conditions. Restrictor temperatures less than 100°C above the melting point of the samples retarded sample transfer into the mass spectrometer, but neither restrictor temperature nor carbon dioxide mobile phase significantly affected negative ion CI conditions.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 23 (1988), S. 204-212 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Collision-induced decomposition/mass-analyzed ion kinetic energy or collisionally activated mass spectra of [M - H]- ions of polyhydroxy compounds and other alcohols and ethers are reported. The [M - H]- ion of each compound is produced under OH- negative ion chemical ionization mass spectrometric conditions. Characteristic fragmentations are observed that include production of [M - H - 2]-, [M - H - 18]- and [M - H - 32]- ions. Certain other fragment ions in the collisionally activated mass spectra make it possible to distinguish among structural isomers. In polyhydroxy compounds, fragmentation increases as the number of hydroxyl groups increase, and carbon-carbon bond cleavage becomes favored.
    Additional Material: 7 Tab.
    Type of Medium: Electronic Resource
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