6533b86cfe1ef96bd12c7ff4
RESEARCH PRODUCT
Thermodynamic Evidence of Cyclodextrin−Micelle Interactions
S. MiliotoNicola MuratoreR. De Lisisubject
chemistry.chemical_classificationAqueous solutionCyclodextrinEnthalpyAlkylationMicelleSurfaces Coatings and FilmsCrystallographychemistryPulmonary surfactantMaterials ChemistryOrganic chemistryPhysical and Theoretical ChemistryEquilibrium constantAlkyldescription
The enthalpy of transfer (ΔHt) of hydroxypropyl-α-cyclodextrin (HP-α-CD), hydroxypropyl-β-cyclodextrin (HP-β-CD), and β-cyclodextrin (β-CD) from water to the aqueous C6F13CO2Na and C7F15CO2Na solutions were determined in the pre- and post-micellar regions. The behavior of the macrocycles is system specific. Generally, the magnitude of the enthalpy is influenced by several factors: (1) the alkyl chain length of the surfactant, (2) the cyclodextrin cavity and its alkylation, (3) the interactions between the free cyclodextrin and the free surfactant, (4) the host−guest equilibrium constant, (5) the host/guest stoichiometry, and (6) the micelle-cyclodextrin (free and/or complexed) interactions. As far as the premicellar region is concerned, HP-α-CD does not form the host−guest complexes. β-CD and HP-β-CD in the aqueous C7F15CO2Na solutions form host−guest complexes of 1:1 stoichiometry; β-CD shows a larger binding affinity toward the surfactant as a compensative effect between the more negative enthalpy and ...
year | journal | country | edition | language |
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2002-08-07 | The Journal of Physical Chemistry B |