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  • Gesamt-, Carbonat- und Nichtcarbonat-C  (1)
  • N ligands  (1)
  • 1
    ISSN: 1434-1948
    Keywords: Carbon dioxide fixation ; Magnesium ; N ligands ; C-C coupling ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The reaction of oxalic amidines R1-N=C(NHR2)-C(NHR2)=N-R1 with CH3MgX followed by uptake of CO2 results in the formation of the trimeric carbamato complexes [R1-N=C(NR2-COO)-C(NR2COO)=N-R1]3Mg3(THF)6 (2a: R1 = R2 = Ph; 2b: R1 = R2 = p-tolyl) as the thermodynamically stable final products of the reaction. Their X-ray crystal structures show that the three metal centres are in a linear arrangement. The central magnesium ion is octahedrally surrounded by six O-donor atoms of the μ2-carbamato bridges, while both peripheral magnesium ions are facially coordinated by three O-donor atoms of the carbamato groups and three THF molecules. This coordination sphere can be considered as a structural model for the active centre in the ribulose-1,5-bisphosphate carboxylase/oxygenase enzyme. Compound 2a reacts with ZnCl2 or CoBr2, with CO2 elimination, to form dimeric complexes of the type [X2M(oxalamidinato)MX2][Mg(DMF)6] (M = Zn, Co; X = Cl, Br). X-ray crystal structure analyses show that the d-metals are tetrahedrally coordinated. The magnesium-bromide-containing intermediates in the formation of 2a and 2b are able to transfer CO2 to acetophenone, thus simulating the CO2 activation step in enzymatic biotin-dependent carboxylation reactions.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Fresenius' Zeitschrift für analytische Chemie 266 (1973), S. 196-201 
    ISSN: 1618-2650
    Keywords: Best. von Kohlenstoff in Gesteinen und Mineralien ; Coulometrische Titration ; Gesamt-, Carbonat- und Nichtcarbonat-C
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Zusammenfassung Für die Bestimmung von Gesamt-, Carbonat- und Nichtcarbonat-Kohlenstoff in magmatischen, metamorphen und sedimentären Gesteinen (auch bei höheren Anteilen an organischem C) ist ein Verfahren nach dem Prinzip der coulometrischen Titration geeignet. Der Gesamt-Kohlenstoff wird ermittelt durch Erhitzung der auf 〈0,125 mm zerkleinerten Probe bei etwa 1250°C im Sauerstoffstrom ohne irgendwelche Zusätze. Zur Bestimmung von Nichtcarbonat-Kohlenstoff wird eine bestimmte Menge Gesteinspulver mit Salzsäure versetzt und auf einem Aluminiumblock HCl abgeraucht. Der Carbonat-Kohlenstoff entweicht als CO2. Zurück bleibt der Nichtcarbonat-Kohlenstoff, welcher wie der Gesamt-Kohlenstoff coulometrisch bestimmt wird. Der Carbonat-Kohlenstoff bzw. die äquivalente Menge CO2 ergibt sich dann aus der Differenz von Gesamt- zu Nichtcarbonat-Kohlenstoff. Das Verfahren ist anwendbar auf Kohlenstoffgehalte in Gesteinen von etwa 10 ppm bis ≧20 Gew.-% bei mittleren Standardabweichungen von etwa 0,0002–0,05% C (Richtwerte). Die Analysendauer für eine Probe beträgt etwa 3–5 min.
    Notes: Abstract For the measurement of total carbon the sample, ground finer than 0.125 mm and without the addition of any reagents, is ignited in a current of oxygen at about 1250°C. Non-carbonate carbon can be analysed after another portion of the sample is treated with conc, hydrochloric acid and evaporated on a hot plate; the carbonates are decomposed and the carbonate carbon is removed as carbon dioxide. The residue is non-carbonate carbon which is also determined by the coulometric method. The difference between total carbon and non-carbonate carbon corresponds to carbonate carbon or its equivalent as carbon dioxide. The method is applicable to carbon contents in rocks from 10 ppm to ≧20 wt.-%. The standard deviation is approximately 0.0002 to 0.05% C. Each carbon analysis takes about 3 to 5 min.
    Type of Medium: Electronic Resource
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