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  • 1
    Electronic Resource
    Electronic Resource
    The influence of acetonitrile on complex formation of crown ethers containing different donor atoms (1988)
    Springer
    Journal of solution chemistry 17 (1988), S. 277-286 
    Details
    ISSN: 1572-8927
    Keywords: Acetonitrile ; crown ethers ; glymes ; alkali metal ions ; calorimetric titrations ; potentiometric titrations ; complex formation ; ligand solvation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The complexation reactions of crown ethers with monovalent cations and Ba2+ were studied in acetonitrile solutions by means of calorimetric and potentiometric titration. The reaction enthalpies measured clearly demonstrate the influence of the interactions between 18-crown-6 and the acetonitrile solvent molecules. Changing the donor atoms or other substituents on the ligand molecule can exert a strong influence on the interactions with the solvent. Thus, all the reaction enthalpies measured for the reaction of 15-crown-5 with different cations are higher compared with 18-crown-6. On comparison with results in methanol, an approximate estimation is made of the influence of solvent molecules on the reaction enthalpies measured in acetonitrile. Due to the strong interaction between silver ion and acetonitrile, complex formation is only observed with crown ethers containing additional nitrogen or sulphur donor atoms.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00646180
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  • 2
    Electronic Resource
    Electronic Resource
    The Complexation of Amino Acids by Crown Ethers and Cryptands in Methanol (1998)
    Springer
    Journal of inclusion phenomena and macrocyclic chemistry 30 (1998), S. 21-28 
    Details
    ISSN: 1573-1111
    Keywords: Amino acids ; crown ethers ; cryptands ; complexes
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Complex formation between several crown ethers and the cryptand (222) and α-amino acids in methanol was studied by calorimetric titration. The ligand structure and the donor atoms of the ligands play an important role in determining the measured values of the reaction enthalpies and entropies. However, with the exception of the diaza crown ether (22) all stability constants are of the same order of magnitude. The enthalpic and entropic contributions to the stabilities of the complexes formed compensate each other. In methanolic solution the amino acids exist in their zwitterionic form. This equilibrium can be influenced. Under acidic, neutral or basic conditions different values of the reaction enthalpies are measured for the complexation of some amino acids with 18-crown-6. These results demonstrate that the concentration of the zwitterionic form of the α-amino acids can be influenced. Thus the reaction between macrocyclic and macrobicyclic ligands and amino acids should be described by at least two different reaction schemes.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1023/A:1007941023186
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    Paper (German National Licenses)
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  • 3
    Electronic Resource
    Electronic Resource
    Synthese und Komplexbildung eines neuen makrocyclischen Liganden mit drei Benzimidazolin-2-on-Einheiten (1992)
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 125 (1992), S. 2483-2485 
    Details
    ISSN: 0009-2940
    Keywords: Macrocyclic ligand ; Benzimidazolin-2-one ; Complexation ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Synthesis and Complex Formation of a New Macrocyclic Ligand Incorporating Three Benzimidazolin-2-one Units The new macrocyclic ligand 1 composed of three benzimidazolin-2-one-1,3-diyl and three propane-1,3-diyl building blocks has been synthesized. Complex formation constants in water involving Li+, Na+, K+, Mg2+ Ca2+, Si2+, and Ba2+ are discussed. The most stable complex is formed with Ca2+.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/cber.19921251121
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    Paper (German National Licenses)
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