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'Electrochemical Reduction' in keywords
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1995 (1)
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1Author    N. B. Mikheev3, A. N. Kam, A. Rum, V. L. Novitschenko3, A. Simon, HjM. AttauschbRequires cookie*
 Title    Electrochemical Cocrystallization Experiments with Gd2Cl3  
 Abstract    G d2Cl3 is electrocrystallized from molten G dC l3 at 900 K with a current efficiency o f 70% referring to the reaction 2G d C l3 + 3 e -= G d2Cl3 + 3 C l-. The reaction is used to determine co­ crystallization coefficients for trivalent rare earths and actinoids (Y, Nd, Cm, Pu), divalent lanthanoids (Eu, Yb), and Sr. The oxidation potential for the above reaction is determined as 2.65 < E ° < 2.68 V. 
  Reference    Z. Naturforsch. 47b, 992—9 (1992); eingegangen am 17. Januar 1992 
  Published    1992 
  Keywords    Cluster, Electrochemical Reduction, Cocrystallization 
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 TEI-XML for    default:Reihe_B/47/ZNB-1992-47b-0992.pdf 
 Identifier    ZNB-1992-47b-0992 
 Volume    47 
2Author    G. Abou-Elenien+, B. Buecher, N. Ismail +++, J. Rieser++, K. WallenfelsRequires cookie*
 Title    Die elektrochemische Reduktion von Benzylidenmalonitrilen The Electrochemical Reduction of Benzylidenemalononitriles  
 Abstract    The influence of different substituents on the electrochemical reduction of benzylidene-malononitriles in benzonitrile at platinium electrodes has been investigated using DC-voltametry, cycl. voltametry and coulometry. 
  Reference    Z. Naturforsch. 38b, 1199—1202 (1983); eingegangen am 16. Juni 1983 
  Published    1983 
  Keywords    Benzylidenemalononitriles, Electrochemical Reduction, DC-Yoltametry, Cycl Voltametry, Coulometry 
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 TEI-XML for    default:Reihe_B/38/ZNB-1983-38b-1199.pdf 
 Identifier    ZNB-1983-38b-1199 
 Volume    38 
3Author    J. G. Assm Ann, J. Voss, G. A. Diw IdjajaRequires cookie*
 Title    Electroreduction of Organic Compounds, 25 [1] Electrochemical Dehalogenation of Chlorinated Insecticides  
 Abstract    Partial but regio-and stereoselective dechlorination takes place if polychlorinated oligo-cyclic insecticides (Diels-Alder adducts and dimers of hexachlorocyclopentadiene) are electrolysed in methanol solution at lead cathodes. The products are detected and identified by GC/MS, IR and NM R spectroscopy. The structure of the product 2 formed from Mirex® is confirmed by an X-ray structural analysis. 
  Reference    Z. Naturforsch. 50b, 953—958 (1995); received November 21 1994 
  Published    1995 
  Keywords    Chlorinated Insecticides, Electrochemical Reduction, Aldrin, Mirex, Dechlorination 
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 TEI-XML for    default:Reihe_B/50/ZNB-1995-50b-0953.pdf 
 Identifier    ZNB-1995-50b-0953 
 Volume    50