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  • Analytical Chemistry and Spectroscopy  (2)
  • Wiley-Blackwell  (2)
  • Blackwell Publishing Ltd
  • Molecular Diversity Preservation International (MDPI)
  • National Academy of Sciences
  • Nature Publishing Group
  • Oxford University Press
  • Wiley
  • 1985-1989  (2)
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  • Wiley-Blackwell  (2)
  • Blackwell Publishing Ltd
  • Molecular Diversity Preservation International (MDPI)
  • National Academy of Sciences
  • Nature Publishing Group
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  • 1
    ISSN: 1052-9306
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Tetrachlorodiphenoquinones have the same exact mass and elemental composition as the toxic environmental contaminant 2,3,7,8-tetrachlorodibenzo-p-dioxin. However, analysis of 3,3′-5,5′-tetrachlorodiphenoquinone showed a pronounced tendency toward chemical reduction in the mass spectrometer to the quinol compound, producing a molecular ion two mass units higher than 2,3,7,8-tetrachlorodibenzo-p-dioxin. Distinct differences were also apparent between the mass spectral fragmentation patterns of 3,3′,5,5′-tetrachlorodiphenoquinone and 2,3,7,8-tetrachloridibenzo-p-dioxin. The 3,3′,5,5′-tetrachlorodiphenoquinone spectrum shows a successive loss of carbon monoxide, with the most prominent fragment corresponding to loss of two molecules of carbon monoxide plus chlorine. In the mass fragmentation of 2,3,7,8-tetrachlorodibenzo-p-dioxin carbon monoxide loss is suppressed, but loss of one molecule of carbon monoxide plus chlorine is a major fragment ion. During an alumina column clean-up procedure 3,3′,5,5′-tetrachlorodiphenoquinone did not coelute with the fraction containing 2,3,7,8-tetrachlorodibenzo-p-dioxin. This evidence indicates that tetrachlorodiphenoquinones are unlikely to interfere with mass spectrometric determination of 2,3,7,8-tetrachlorodibenzo-p-dioxin in environmental samples.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Chichester [u.a.] : Wiley-Blackwell
    Journal of Raman Spectroscopy 16 (1985), S. 272-279 
    ISSN: 0377-0486
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Systems of copper(I), silver(I) and gold(I) cyanides dissolved in aqueous solutions of sodium thiosulphate in different molar ratios have been studied by Raman Spectroscopy. CuCN dissolves completely in aqueous thiosulphate solution in a 1:3 CuCN to S2O32- ratio, forming only mixed cyanothiosulphate species. No evidence was found for the formation of Cu (CN)2-, Cu(CN)32- or Cu(CN)43-. The mixed cyano copper complex was isolated as a white solid insoluble in water and most other solvents. The solid probably consists of a polymeric structure with bridging cyanide and thiosulphate. AgCN dissolves completely in aqueous thiosulphate solution in a 1:1 AgCN to S2O32- ratio, resulting in the formation of Ag(CN)2- and Ag(S2O3)23- species. As the concentration of thiosulphate increases Ag(CN)2(S2O3)3- and Ag(CN)2(S2O3)25- are formed. There is strong evidence for the existence of bridging silver thiosulphate complex in solutions of low S2O32- concentration. AuCN dissolves completely in aqueous thiosulphate solution in a 1:2 AuCN to S2O32- ratio, forming Au(CN)2-, Au(CN) (S2O3)2- and Au(S2O3)23-. No evidence was found for the formation of species of higher coordination number on increasing the concentration of S2O32-, which indicates that the linear two-coordinate gold complexes are the most stable.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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