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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Journal of inclusion phenomena and macrocyclic chemistry 23 (1995), S. 73-82 
    ISSN: 1573-1111
    Keywords: Aminimide ; extraction ; heavy metal cations
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The title compounds were prepared in good yields by Slagel's method. All compounds obtained were used as agents for liquid-liquid extraction. They showed high affinity for certain heavy metal cations and their extractability depended to a great extent on the ligand structure. This dependence is believed to be due to the chelation of the metal cations between the imino nitrogens and the additional ligating site.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Journal of inclusion phenomena and macrocyclic chemistry 23 (1995), S. 329-341 
    ISSN: 1573-1111
    Keywords: Ion cleft ; three-bridged cyclophane ; crownophane ; extraction ; metal cation ; ester ; pyridyl group ; aminimide
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract A variety of new three-bridged cyclophanes, clefts4–14, have been conveniently prepared, and their cation-binding properties have been examined. Compounds4–6 have a special affinity for alkali metal cations. Ethyl ester5 and methyl ester4 selectively formed 2:1 complexes with K+ and Na+ ions, respectively. Clefts11–13, which possess pyridyl groups, bind Ag+ cation exclusively.1H NMR titration studies confirmed that11 or12, having 2- or 3-pyridyl groups, form a 1:1 complex with Ag+ cation, while13, with 4-pyridyl ligating groups, forms a 2:1 complex. Cleft10, with aminimide groups, also shows an affinity for Ag+ cation in a 2:1 ratio in a polar solvent, while it forms a 1:1 complex in a nonpolar solvent. The same solvent effect was observed for clefts13 and15c, which is discussed qualitatively.
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Journal of inclusion phenomena and macrocyclic chemistry 19 (1994), S. 41-53 
    ISSN: 1573-1111
    Keywords: Syn-conformer ; cyclophane ; metal ion ; extraction ; catalytic activity
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Rigidified calix[4]arene analogs were synthesized fromsyn-[2.n]metacyclophanes as a building block. Their structure was firmly locked in the cone conformation. An enlarged calix[4]arene analog was obtained after the cyclobutane ring cleavage of the parent analog by Birch reduction. Several ionophores have been derived from the analogs and been found to select the larger ions during the extraction of alkali metals, transition metals, and lanthanoids. The ionophore having oligoethylene glycol units showed an effective catalytic activity for SN2 reactions such as ester synthesis, Williamson ether synthesis, and Finkelstein reaction in several media.
    Type of Medium: Electronic Resource
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