Volume 95 Issue 39 | p. 11 | Concentrates
Issue Date: October 2, 2017

Radical reaction caught on the rebound

With FeOH model system, chemists observe key step in hydroxylation of C–H bonds for the first time
Department: Science & Technology
News Channels: Biological SCENE
Keywords: Reaction mechanisms, radical rebound, cytochrome P450
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This model system makes it possible to observe the radical rebound reaction (C is gray, H is white, N is blue, O is red, Fe is orange).
Credit: Paulo Zaragoza
A 3-D structure of a new model system that makes it possible to observe the radical rebound mechanism.
 
This model system makes it possible to observe the radical rebound reaction (C is gray, H is white, N is blue, O is red, Fe is orange).
Credit: Paulo Zaragoza

For more than 40 years, chemists and biologists have used the radical rebound mechanism to describe what happens when enzymes with transition metals, such as cytochrome P450, hydroxylate C–H bonds. Such enzymes first remove a hydrogen atom from a C–H bond using a high-valent metal-oxo species. This produces a carbon radical and a metal-OH intermediate that then rebounds—the hydroxyl group moves onto the carbon radical and the metal is reduced by one electron. Although plenty of circumstantial evidence suggests this is what happens, observing the rebound step in this reaction has been impossible because it is fast compared with the hydrogen atom removal step. Now, chemists led by David P. Goldberg of Johns Hopkins University have created the first model system in which the rebound reaction can be observed (J. Am. Chem. Soc. 2017, DOI: 10.1021/jacs.7b07979). The system features Fe–OH ensconced in a tris(triphenyl)phenyl corrole ligand, which stabilizes the high redox level of the Fe complex and has sufficient steric bulk to prevent dimerization—a problem that often plagues FeOH systems. “In our case, the rebound reaction is best described as a concerted process as opposed to a stepwise process,” Goldberg says. Such mechanistic insight, he adds, could be used to engineer an enzyme or synthetic catalyst to facilitate or inhibit the rebound step and thereby influence the efficiency and selectivity of the hydroxylation.

 
Chemical & Engineering News
ISSN 0009-2347
Copyright © American Chemical Society

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