Abstract
A novel macrocyclic host molecule was synthesized that forms in a single step from commercially available starting materials. The core of the macrocycle backbone possesses two quinone rings and, thus, it is redox-active. Host–guest binding involving the clip-shaped cavity indicates selective binding of pyridine N-oxides based on the electron density of and steric bulk around the anionic oxygen.
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Petersen, R. J., Rozeboom, B. J., Oburn, S. M., Blythe, N. J., Rathje, T. L., Luna, J. A., … Wackerly, J. W. (2020). Cambiarenes: Single-Step Synthesis and Selective Zwitterion Binding of a Clip-Shaped Macrocycle with a Redox-Active Core. Chemistry - A European Journal, 26(9), 1928–1930. https://doi.org/10.1002/chem.201904852
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