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  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Journal of High Resolution Chromatography 10 (1987), S. 263-268 
    ISSN: 0935-6304
    Keywords: Gas chromatography ; Fused silica capillaries ; Automated cold on-column injection ; High oven temperature ; Lipid analysis ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Modification of the Carlo-Erba cold on-column injector for (automated) analysis of high molecular compounds at high oven temperature is described. The secondary cooling tube of the cold on-column injector is replaced by a lengthened tube through which a high air flow is directed. The injection site is maintained at 65-70 °C while the oven is at high temperature (≷ 300 °C). For automated injection, a short deactivated precolumn of 22 to 30 cm × 0.53 mm i.d. is coupled to the analytical column via a butt connector with make-up gas supply. For a triglyceride mixture, automatically injected at 300 °C, the mean % deviation for all peak areas was 1.8% and the mean % deviation for all retention times was 0.09 % for five consecutive runs.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 25 (1987), S. 179-180 
    ISSN: 0749-1581
    Keywords: 13C NMR ; 4-substituted phenacyl chlorides and iodides ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The 13 NMR singles for some 4-substituted phenacylchlorides and iodides were assigned. The carbonyl carbons exhibit upfield shifts compared with those of the corresponding 4-substituted acetophenones; in the chlorinated derivatives a downfield shift is observed for the α-methylene carbons, while a reverse effect occurs in the iodinated compounds. The chemical shifts of the aromatic ring carbons are in close agreement with those calculated using substituent chemical shifts.
    Additional Material: 3 Tab.
    Type of Medium: Electronic Resource
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