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Cambiarenes: Single-Step Synthesis and Selective Zwitterion Binding of a Clip-Shaped Macrocycle with a Redox-Active Core. Chemistry 2020 Feb 11;26(9):1928-1930

Date

11/07/2019

Pubmed ID

31696566

DOI

10.1002/chem.201904852

Scopus ID

2-s2.0-85078876290 (requires institutional sign-in at Scopus site)   2 Citations

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.

Author List

Petersen RJ, Rozeboom BJ, Oburn SM, Blythe NJ, Rathje TL, Luna JA, Kibby SK, O'Brien EA, Rohr KG, Carpenter JR, Sanders TL, Johnson AM, Hutchins KM, Shaw SK, MacGillivray LR, Wackerly JW

Author

Riley J. Petersen PhD, BA Postdoctoral Researcher in the Biophysics department at Medical College of Wisconsin