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  • 1
    ISSN: 1573-1111
    Keywords: Crown ether-primary ammonium cation complexation ; formation constants (K) ; enthalpy changes (ΔH) ; entropy changes (ΔS) ; titration calorimetry
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Equilibrium constant (K), enthalpy change (ΔH), and entropy change (ΔS) values have been determined calorimetrically at 25°C in 90%MeOH 10%H2O (v/v) for the interactions of pyridino-18-crown-6 (P18C6) and diketopyridino-18-crown-6 (K2P18C6) with perchlorate salts of ammonium, benzylammonium,α-phenylethylammonium,β-phenylethylammonium, andα-(1-naphthyl)ethyl-ammonium cations. The crystal structure of the complex of P18C6 with benzylammonium perchlorate was determined by X-ray crystallography. The1H 1D and 2D NMR spectra of some of these complexes were used to elucidate their structural features in solution. The logK values for the interaction of the ammonium cations with P18C6 are larger than those with K2P18C6, probably due to the higher degree of structural flexibility of P18C6. Ligand K2P18C6 displays appreciable π-π interaction with theα-(1-naphthyl)ethylammonium cation, but not with theα-phenylethylammonium cation.
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Journal of inclusion phenomena and macrocyclic chemistry 12 (1992), S. 275-289 
    ISSN: 1573-1111
    Keywords: Crown ether-ammonium cation complexation ; formation constants (K) and enthalpy changes (ΔH) ; direct1H NMR method ; titration calorimetric method
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract A direct1H NMR method for determining logK and ΔH values for crown ether-ammonium cation complexation using milligrams of sample was tested and evaluated for accuracy and precision by comparing the results with those obtained using a titration calorimetric method. LogK values for the interactions of a non-chiral crown ether, diketopyridino-18-crown-6 (K2P18C6), with α-phenylethylammonium (PhEt+) perchlorate in 50%–50% and 90%–10% (v/v) mixtures of deuterated methanol (CD3OD) and deuterated chloroform (CDCl3) at four temperatures and, with α-(1-naphthyl)ethylammonium (NapEt+) perchlorate in 50%CD3OD-50%CDCl3 (v/v) at 25°C were determined by a direct1H NMR method. Values of ΔH for the interactions of K2P18C6 with PhEt+ in the two solvents were calculated from the temperature dependence of logK. LogK values for the interactions of a chiral crown ether, dimethyldiketopyridino-18-crown-6 (M2K2P18C6), with (R) and (S) enantiomers of NapEt+ in pure CD3OD at 25.0°C were also determined by the NMR method. The results were compared with those determined by a calorimetric method at 25.0°C in 50%-50% and 90%–10% (v/v) mixtures of plain methanol and chloroform, in 100% plain methanol, and in a 50%-50% mixture of partially deuterated methanol (with deuterium substitution on the methanol OH group, CH3OD) and deuterated chloroform. The log K values determined by both methods were found to be in good agreement, but the standard deviations associated with the NMR logK values were two to three times greater. The agreement of the ΔH values determined by the two methods was poor, differing by approximately 10 kJ/mol with the NMR method giving more negative values. The standard deviations associated with the NMR ΔH values were approximately ten times greater than those for the calorimetric values. Ion-pairing was observed for the interaction of perchlorate ion with both free and bound PhEt+ in 50%methanol-50%chloroform mixture. It is concluded that the NMR procedure is satisfactory for the determination of logK, but not ΔH values.
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