| Autor: |
Ngai C; Department of Chemistry and the UC Riverside Center for Catalysis, University of California, Riverside, Riverside, California 92521, United States., da Camara B; Department of Chemistry and the UC Riverside Center for Catalysis, University of California, Riverside, Riverside, California 92521, United States., Woods CZ; Department of Chemistry and the UC Riverside Center for Catalysis, University of California, Riverside, Riverside, California 92521, United States., Hooley RJ; Department of Chemistry and the UC Riverside Center for Catalysis, University of California, Riverside, Riverside, California 92521, United States. |
| Abstrakt: |
A self-assembled Fe 4 L 6 cage with internally oriented carboxylic acid functions was shown to catalyze a variety of dissociative nucleophilic substitution reactions that proceed via oxocarbenium ion or carbocation intermediates. The catalytic behavior of the cage was compared to that of other small acid catalysts, which illustrated large differences in reactivity of the cage-catalyzed reactions, dependent on the structure of the substrate. For example, only a 5% cage confers a 1000-fold rate acceleration of the thioetherification of vinyldiphenylmethanol when compared to the rate with free carboxylic acid surrogates but only a 52-fold acceleration in the formation of small thioacetals. Multiple factors control the variable reactivity in the host, including substrate inhibition, binding affinity, and accessibility of reactive groups once bound. Simple effective concentration increases or the overall charge of the cage does not explain the variations in reactivity shown by highly similar reactants in the host: small differences in structure can have large effects on reactivity. Reaction of large spherical guests is highly dependent on substitution, whereas flat guests are almost unaffected by size and shape differences. The cage is a promiscuous catalyst but has strong selectivity for particular substrate shapes, reminiscent of enzymatic activity. |
