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  • Crown ether  (1)
  • Ion-pair solvation complexes  (1)
  • glyme-separated ion pairs  (1)
  • 1
    ISSN: 1572-8927
    Keywords: Optical spectroscopy ; bolaform electrolytes ; ion pairs ; ion-pair aggregation ; glyme-separated ion pairs ; α,ω-(9-fluorenylsodium)-polymethylenes ; fluorenylsodium ; tetraglyme ; tetrahydrofuran ; tetrahydropyran
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Formation constants of tetraglyme (glyme 5) separated ion pairs of bolaform electrolytes of the type Na+,−Fl(CH2) n Fl−, Na+ (Fl− denoting a fluorenyl carbanion) were measured spectrophotometrically in tetrahydrofuran (THF) and tetrahydropyran (THP) at 25°C as a function of the chain lengthn, withn=2, 3, 4, or 6. The ratiosK 1/K 2 of the first and second glyme ion-pair separation steps were found to be equal to the statistical factor 4 in all cases except in THP for the compoundn=2, where the ratio is 15. Values ofK 1 as well as K 2 increase considerably with chain length, the former by a factor 19 asn increases from 2 to 6. The ion-pair separation with glyme 5 is easier in THP than in THF. The results are discussed in terms of differences in external cation solvation and the possible involvement of cyclized structures or curled conformations as a result of interactions between the terminal ion pairs.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Journal of inclusion phenomena and macrocyclic chemistry 3 (1985), S. 197-208 
    ISSN: 1573-1111
    Keywords: Crown ether ; binding constants ; polystyrene ; networks
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The binding constants,K N, of sodium and potassium 8-anilinonaphthalene-1-sulfonate (ANS) and of sodium 5-dimethylamino-1-naphthalenesulfonate (DNS) to benzo-18-crown-6 bound to a 2% cross-linked polystyrene network (RN18C6) were measured spectrophotometrically in dioxane and the results compared with those obtained for picrate salts. The network RN18C6 was then used to measure in dioxane and toluene by a competition method the equilibrium constant,K, of the reaction A−M+N+Cr⇄A−M+Cr+N.A−M+N denotes the ionic solute (ANS, DNS, methyl orange or picrate salt) bound to the network RN18C6 (N) and A−M+Cr is the solute bound to a soluble ligand Cr, where Cr represents a series of 18-crown-6 and 15-crown-5 compounds. Combining theK N andK values the formation constants,K L, of the crown ether complexes of the respective salts were obtained in dioxane. The data show a reversal in the complexation strength of the 18-crown-6 compounds in dioxane when sodium picrate is replaced by sodium ANS. The results were rationalized in terms of a synergistic effect exerted by dioxane, with dioxane forming a 1:1 dioxanate with the crown ion pair complex. This effect is especially strong with ANS and with a rigid planar crown ether like dibenzo-18-crown-6. The binding constants,K N, of NaANS and NaDNS to RN18C6 in dioxane are nearly three times larger than for sodium picrate, and the same holds for the potassium salts. Differences in anion interactions with the network appear to be a plausible cause for the anion dependence ofK N.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 0570-0833
    Keywords: Ion-pair solvation complexes ; Solvation complexes ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: In solvents of low polarity, salts containing a carbanion, e.g. fluorenylsodium, or a radical anion, e.g. coronenesodium, can exist as contact ion pairs or as solvent separated ion pairs. Particular interest attaches to the complexes of ion pairs with the strongly solvating, polydentate polyglycol dimethyl ethers (glymes) and with crown compounds. These systems can be studied by optical spectroscopy, NMR spectroscopy, and other methods.
    Additional Material: 15 Ill.
    Type of Medium: Electronic Resource
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