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- W2002015209 abstract "A 19F NMR chemical shift study of a homologous series of perfluorocarbon (fc) [CxF2x+1CO2Na, x = 3, 4, 6−9] surfactants (S) has been carried out in D2O and in binary solvent (D2O + cyclodextrin (CD)) systems at 22 °C. Both β-CD and modified cyclodextrins were used. Complementary 1H NMR chemical shift data for the cyclodextrins in binary solvent (D2O + S) systems were also obtained. Values of the complex-induced chemical shifts (CIS) for selected host or guest nuclei are observed to increase with increasing alkyl chain (Cx) length of the surfactant when the CD/S complex has a 1:1 stoichiometry. However, for complexes having stoichiometries other than 1:1 CD/S, somewhat different trends in the CIS values were observed. Binding constants (Ki) have been obtained from the analysis of 19F and 1H CIS values of the CD/S systems using equilibrium models in which 1:1, 1:1 plus 2:1, 1:1 plus 1:2 complexes, and uncomplexed species are present. In general, Ki increases as Cx increases; however, differences in the binding affinity, stoichiometry, and inclusion geometry of the CD/S complexes were observed to depend on the type of cyclodextrin. The latter can be understood in terms of the steric effects created by the introduction of alkyl groups in the annulus region of the cyclodextrin." @default.
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- W2002015209 date "1998-08-01" @default.
- W2002015209 modified "2023-10-07" @default.
- W2002015209 title "<sup>19</sup>F and <sup>1</sup>H NMR Investigation of Cyclodextrin/Fluorocarbon Alkyl Carboxylate Surfactant Inclusion Complexes" @default.
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- W2002015209 doi "https://doi.org/10.1021/la9802365" @default.
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