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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Journal of inclusion phenomena and macrocyclic chemistry 10 (1991), S. 79-96 
    ISSN: 1573-1111
    Keywords: Inclusion complexes ; β-cyclodextrin host ; β-cyclodextrin polymer host ; ferrocene guest ; 2-, 3-, 4-nitroaniline guests ; 2-, 3-, 4-nitrotoluene guests ; 2-, 3-, 4-nitrophenol guests ; 3,4- and 3,5-dinitrotoluene guests ; 2-, 3-, 4-chloronitrobenzene guests ; 2- and 4-nitrobenzoic acid guests ; chemically modified (β-cyclodextrin polymer)-PTFE-carbon composite electrode ; hopping mechanism of diffusion of a guest species between polymer inclusion sites
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Host-guest equilibria have been investigated involving inclusion sites of the microparticulate amorphous β-cyclodextrin polymer, β-CDP-25, and a range of redox guests comprising regioisomeric nitrobenzene derivatives and ferrocene. The equilibria were studied by the batch method. Inclusion-governed, Langmuir-type sorption equilibria occurred in the β-CDP-25/guest systems studied in 1:1 (v/v) aqueous methanolic solutions. A 1:1 (host inclusion site)/guest stoichiometry was found and sorption equilibrium constants were determined. The values of the constants changed by a factor of 20 between the most weakly and strongly included guests. Regioselective discrimination of β-CDP-25 was most pronounced with respect to nitrophenols. Transport phenomena of guest molecules in the β-CDP-25 matrix have also been studied. The apparent diffusion coefficients of guest molecules were determined in the β-CDP-25 matrix by chronamperometry at the (β-CDP-25)-PTFE-carbon composite electrodes. These diffusion coefficients were almost four orders of magnitude lower than the corresponding coefficients of guest molecules in solution in the absence of β-CD. The diffusion mechanism was postulated for the guest molecules in the β-CDP-25 matrix, which invoked hopping of the molecules between inclusion sites.
    Type of Medium: Electronic Resource
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