Formation of distinct iron hydrides via mechanistic divergence in directed C-H Bond activation of aryl ketones, esters and amides

Directing groups play an important role in controlling the selectivity of C-H bond activation. Here we demonstrate that for iron, the nature of the directing group (e.g., ketone, ester, or amide) influences the C-H activation process. In this study the C-H bond activation step either occurs with or without the assistance of the directing group resulting in distinct cis- and trans-isomers of the corresponding iron hydride.

Automated summary

Directing groups are crucial for controlling the selectivity of C-H bond activation. In this study, we show that the nature of the directing group (ketone, ester, or amide) influences the C-H activation process for iron, leading to distinct cis- and trans-isomers of the corresponding iron hydrides.