The inclusion complexes between the most commonly used cyclodextrins (alpha-, beta-, and gamma-CD) and 1-bromoadamantane were prepared and studied experimentally by NMR methods and by molecular dynamics simulations (AMBER force field) with solvation. The NMR results suggest host/guest ratios of 2:1, 1:1, and 1:1 for the complexes with alpha-, beta-, and gamma-cyclodextrin, respectively, as well as defined geometries for the complexes. Averaged geometrical data from the molecular dynamics simulations agree with the complexation geometries deduced experimentally.
Methylene chloride (CH2Cl2) is a representative model compound commonly found in aqueous
wastes, process effluents, and contaminated soils and sediments. Oxidation in supercritical water
provides a viable treatment and remediation pathway to convert CH2Cl2 to CO2, H2O, and HCl.
However, in earlier work, partial hydrolysis was observed at subcritical temperatures (<374
°C). This low-temperature reactivity complicates the measurement of kinetic data. In this study,
the kinetics of CH2Cl2 hydrolysis in sub- and supercritical water were experimentally measured
and modeled. Catalytic effects from a high nickel content alloy used for the reactor were studied
by comparing kinetic data obtained in quartz ampules with and without metal present. No
heterogeneous catalysis effects were observed. Reaction rates from 100 to 500 °C were measured
to check the reproducibility of existing published data (up to 150 °C) and to extend the database
for hydrolysis to the supercritical region in order to develop a robust empirical global rate
expression. The data show a local maximum in the rate constant below the critical point of
water, consistent with a possible change in the reaction mechanism induced by changes in the
solvent's physical properties (dielectric constant, density, etc.). Variations in the global rate
constant agree quantitatively with predictions obtained by applying the Kirkwood model, which
accounts for changes in the dielectric constant and density of the solvent.
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