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Updated: Aug 29, 2025

Line Shape Analysis of Dynamic NMR Spectra for Characterizing Coordination Sphere Rearrangements at a Chiral Rhenium Polyhydride Complex
Published on: July 27, 2022
Tuning through-space interactions via the secondary coordination sphere of an artificial metalloenzyme leads to
Isra S Hassan1, Jack T Fuller2, Vanessa N Dippon1
1Department of Chemistry, Columbia University New York NY 10027 USA tr2504@columbia.edu.
Abstract:
We report computationally-guided protein engineering of monomeric streptavidin Rh(iii) artificial metalloenzyme to enhance catalysis of the enantioselective coupling of acrylamide hydroxamate esters and styrenes. Increased TON correlates with calculated distances between the Rh(iii) metal and surrounding residues, underscoring an artificial metalloenzyme's propensity for additional control in metal-catalyzed transformations by through-space interactions.
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