Library

feed icon rss

Your email was sent successfully. Check your inbox.

An error occurred while sending the email. Please try again.

Proceed reservation?

Export
Filter
  • preferential solvation  (3)
  • 14N,2H,23Na+,133Cs+ NMR  (1)
  • Dimethylacetamide-water mixtures  (1)
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Journal of solution chemistry 19 (1990), S. 193-205 
    ISSN: 1572-8927
    Keywords: Dimethylacetamide-water mixtures ; rotational molecular motion ; solvent-solvent interaction ; 14N,2H,23Na+,133Cs+ NMR ; Na+ and Cs+ solvation ; preferential solvation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Nuclear magnetic relaxation by intra- and intermolecular quadrupoleelectric field gradient interaction has been used for the study of the systems DMA-water-NaI and DMA-water-CsI at 25°C.14N relaxation of DMA and2H relaxation of D2O measured over the complete mixture range reveal the behavior of the rotational molecular motion of the two solvent components. For both solvent components a marked maximum of the reorientational correlation time has been found, reflecting hydrophobic effects and strong DMA-water interaction. The quadrupolar relaxation rates of23Na+ and133Cs+ in pure DMA were evaluated giving an indication that the electric solvent dipoles in the solvation shell are not located on positions of cubic symmetry. A quantitative study of preferential solvation of the cations in the mixed solvent has been performed by using the H2O-D2O isotope effect on23Na+ and133Cs+ relaxation. For both cations an obviously typical change in the selectivity occurs. In the range l〉x H2 O〉0.7 we find weak preferential hydration, but in the range 0.7〉xH 2 O〉0 strong preferential solvation by DMA is reflected.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 2
    ISSN: 1572-8927
    Keywords: Quadrupole relaxation ; 23Na+,87Rb+, and14N NMR ; ion-solvent interaction ; asymmetry effects ; preferential solvation ; acetonitrile-water mixtures
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Nuclear magnetic relaxation rates of23Na+,87Rb+, and14N in acetonitrile-water mixtures have been measured over the complete mixture range. The interaction of the quadrupole moment of ionic nuclei with electric field gradients is an excellent short ranged probe for the direct neighborhood of ions in solution. Thus the23Na+ and87Rb+ relaxation contains information about dynamics composition and symmetry of the inner solvation sphere in the mixed solvent. It was found that the relaxation rate of both ionic nuclei has an unexpected marked maximum in the acetonitrile (AN) rich region. The14N and2H relaxation rates of the solvent molecules revealed that the maximum could not be explained by dynamic effects. Further experimental results showed that it is caused by local symmetry changes. By measuring 1/T1 of the cationic nuclei in AN-H2O and AN-D2O it was possible for the first time to separate quantitatively asymmetry effects from selective solvation effects. It turned out that both cations are strongly preferentially hydrated. Comparison of the results of two approaches for the evaluation of the D2O-H2O isotope effect led to interesting hints concerning the location of the electric point dipole in acetonitrile molecules having contact with cations.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Journal of solution chemistry 7 (1978), S. 705-720 
    ISSN: 1572-8927
    Keywords: 23Na+ and81Br− NMR relaxation ; ion-solvent interactions ; preferential solvation ; H2O + amide mixtures ; hydrophobic effects ; formamide ; N-methylformamide ; N,N-dimethylformamide
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Ion-solvent interactions of Na+ and Br− in binary aqueous mixtures of formamide,N-methylformamide (NMF), andN,N-dimethylformamide (DMF) are studied by use of23Na and81Br magnetic relaxation times, extrapolated to zero salt concentration. The relaxation times, which are controlled by quadrupolar interaction, have been measured over the complete mixture range and are compared with a simplified theoretical formula. It turned out that the23Na+ relaxation in H2O-formamide and H2O-NMF mixtures is in excellent agreement with theoretical predictions, implying nonpreferential solvation of Na+ in these systems. Small deviations of experimental from theoretical results in H2O+DMF possibly indicate weak selective hydration of the cation. In the case of the anionic nuclei81Br−, deviations from the theoretical curve occur which are to be expected, especially for systems where hydrophobic effects play a role. On the other hand, it is demonstrated that these deviations can easily be explained within the electrostatic theory by differences in structural details of the anionic solvation sphere in the mixtures compared to the pure solvents.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...