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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 90 (1986), S. 4618-4621 
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    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
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 22 (1984), S. 3001-3010 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The binding of 41-(1-pyrenyl)butyltrimethylammonium bromide (PN+) to the neutral poly-soap-type polymers poly(vinylbenzo-18-crown-6) (P18C6) and poly(vinylbenzoglyme) (PVBG) was studied by optical spectroscopy and fluorescence in the presence and absence of salts. Measurements of the respective binding constants were based on distinct differences in the optical absorption spectra of free and polymer-bound PN+. When crown ether-compelxable cations (e.g., K+) were added the adsorption of PN+ to P18C6 decreased as the neutral polymer was converted to a polycation. No decrease was found with PVBG because alkali ions do not complex significantly to this polymer in water. PN+ adsorption to both polymers rose rapidly, however, as the salt concentration increased. This effect was strongly anion-dependent and increased in the order of Cl- 〈 Br- 〈 I- 〈 CNS- 〈 BPh4-. The increased binding was reflected in a higher binding constant and also in a larger number of bound PN+ molecules per polymer chain under saturation conditions. It is argued that the formation of ion pairs or larger ion clusters in the aqueous phase when anions are added forces more PN+ molecules to adsorb on the surface of the polymer coil to which they are bound as ion pairs or higher aggregates. Under saturation conditions enough PN+ molecules are bound to convert the pyrene monomer fluorescence spectrum into that of the excimer. These results are compared with data obtained for the anionic solute 4-(1-pyrenyl)butanoate in the presence of salts.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Oligo(oxyethylene)s immobilized as pendant groups on a polymethacrylate-based resin were used as phase transfer catalysts in the reaction of solid alkali phenoxides with octyl halides in toluene and in the synthesis of benzyl acetate from benzyl bromide and solid alkali acetates in chloroform. The resins are cross-linked homopolymers or copolymers of methyl ethers of oligo(ethylene glycol) methacrylates of the general formula H2C=C(CH3)COO(CH2CH2O)n CH3 with n = 4 (MG4), 8 (MG8) or 22 (MG22), the comonomers being styrene, methyl methacrylate (MMA), acrylonitrile or 4-vinylpyridine. The conversion of the organic halides into the respective products were found to be all pseudo first order reactions and the observed rate constants are proportional to the amount of added catalyst and decrease with increasing crosslinking density of the catalyst. Catalysts with longer oligo(oxyethylene) chains have considerably higher activity. Incorporation of more than 50 mol-% MMA comonomer decreases the catalytic activity at least for the benzyl bromide reaction, but the structure of the comonomer has no significant effect. The catalysts are easily synthesized in large quantities from commercially available monomers.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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