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  • acetonitrile  (2)
  • 1:1 electrolytes  (1)
  • 1
    Digitale Medien
    Digitale Medien
    Conductivities of 1∶1 salts in 2-cyanopyridine (1994)
    Springer
    Journal of solution chemistry 23 (1994), S. 579-593 
    Details
    ISSN: 1572-8927
    Schlagwort(e): 2-Cyanopyridine ; conductivities ; 1∶1 electrolytes ; dilute solutions ; single ion molar conductivities ; ion association ; mixed solvents ; acetonitrile ; concentrated solutions ; LiAsF6 ; high energy density lithium batteries
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Chemie und Pharmazie
    Notizen: Abstract Electrolytic conductivities of eight simple 1∶1 electrolytes have been measured in dilute solutions of 2-cyanopyridine (2CNP) at 30°. Infinite dilution mobilities and association constants were calculated using the Fuoss-Hsia equation. With the exception of LiCF3SO3 all salts show very little association, consistent with the very high dielectric constant of 2CNP. The weak association which does occur is attributed to weak ion-solvent interactions. No evidence was found for triple ion formation. Conductivities of concentrated solutions of LiAsF6 in 2CNP increase slowly with concentration reaching a maximum at a concentration of around 0.65 mol-dm−3. These conductances are slightly lower than those in propylene carbonate which has a lower dielectric constant and a higher viscosity. Conductivities of concentrated LiAsF6 solutions in 2CNP mixtures with acetonitrile vary monotonically, consistent with solution viscosities, and show no sign of the maximum commonly observed in mixed organic solvents.
    Materialart: Digitale Medien
    URL: http://dx.doi.org/10.1007/BF00972746
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 2
    Digitale Medien
    Digitale Medien
    Conductance of 1:1 electrolytes in methyl formate (1987)
    Springer
    Journal of solution chemistry 16 (1987), S. 225-235 
    Details
    ISSN: 1572-8927
    Schlagwort(e): Conductivities ; 1:1 electrolytes ; methyl formate ; ion pairs ; triple ions ; ion solvation
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Chemie und Pharmazie
    Notizen: Abstract The electrolytic conductivities of LiClO4, LiAlCl4, LiAsF6, NaClO4, NaBPh4, and Bu4NClO4 have been measured in methyl formate at 25°C. Evidence is presented for strong association between the perchlorate ion and the formyl proton of the solvent. Ion association and triple ion formation constants suggest that LiClO4, LiAlCl4, and NaClO4 form solvent separate ion pairs and triple ions. NaBPh4 forms contact ion pairs and triple ions, and the remaining salts appear to form both types of ion pairs and triple ions.
    Materialart: Digitale Medien
    URL: http://dx.doi.org/10.1007/BF00646988
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  • 3
    Digitale Medien
    Digitale Medien
    Complexation of alkali metal cations by calix[4]Arene-bis-crown-6 in methanol, acetonitrile and propylene carbonate (1996)
    Springer
    Journal of solution chemistry 25 (1996), S. 955-970 
    Details
    ISSN: 1572-8927
    Schlagwort(e): Electrolytic conductance ; molar conductance ; ion pair formation ; complex formation ; 18-crown-6 ; calix[4]arene-bis-crown-6 ; lithium perchlorate ; sodium perchlorate ; potassium perchlorate ; rubidium perchlorate ; cesium perchlorate ; acetonitrile ; methanol ; propylene carbonate
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Chemie und Pharmazie
    Notizen: Résumé The interactions of Li+, Na+, K+, Rb+, and Cs+ with the “double-crown calix,” calix[4]arene-bis-crown-6, have been studied in methanol, acetonitrile, and propylene carbonate at 25°C using precise conductivity measurements. For Li+ and Na+ in solutions containing this calix[4]arene, only 1:1 cation:ligand complexes are formed which permit the determination of the thermodynamic complexation formation constants,K f. The conductivity data strongly suggest that 2:1 cationcalixarene complexes form with K+, Rb+, and Cs+. The existence of 2:1 complexes was experimentally confirmed for the potassium systems by a mass spectroscopic method.
    Materialart: Digitale Medien
    URL: http://dx.doi.org/10.1007/BF00972592
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