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  • Chemistry  (2)
  • 1
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 6 (1972), S. 843-851 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The individual, deuterated, isomeric α- and β-carotenes were isolated from the green alga, Scenedesmus obliquus, cultivated in D2O containing 99·7 to 99·8 atom percent deuterium. Mass spectroscopy showed that both the α- and β-deuterio-carotene preparations contained principally the fully deuterated pigment molecules (C40D56), small quantities of deuterated molecules with one proton (C40D55H) and yet smaller quantities of deuterated molecules with two protons (C40D54H2). From statistical calculations the deuterio-carotene preparations also contained one to several isotopically-substituted deuterio-carotenes of each mass in the mass range 585 to 599 because of variation of the number of 13C and H atoms per molecule. The mass fragmentation of the deuterated pigments was analogous to that of the respective ordinary α- and β-carotene. It indicated that the protons in the C40D55H and C40D54H2 molecules were distributed approximately randomly in various parts of the structure as in the terminal rings and in the ends and central portions of the polyene chain.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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  • 2
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 5 (1971), S. 565-572 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: High resolution mass spectrometry has been employed to establish the structural formulae of the unique carotenoid pigment siphonaxanthin, its natural ester, siphonein and several derivatives. Siphonaxanthin exhibits a fragmentation reaction that is unusual among carotenoid pigments, namely, the elimination of carbon dioxide, observed as [M - CO2] and [M - (CO2 + H2O)]. This reaction involves the migration of an oxygen atom. Siphonaxanthol, a partially hydrogenated siphonaxanthin, exhibits a similar reaction involving the elimination of carbon monoxide and formaldehyde. From the fragmentation of derivatives of siphonaxanthin, such as the triacetate, the dimethyl ether and siphonaxanthol, and also from the fragmentation of related pigments, such as loroxanthin and fucoxanthin, the unique structural units responsible for the elimination of the carbon dioxide and carbon monoxide have been identified.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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