An Achiral Tetradentate Cis‐α‐Coordinating NCCN Ligand Gives Rise to a Configurationally Stable Chiral‐at‐Iron Complex for Enantioselective Catalysis
Lukas Hinterlang, Nemrud Demirel, Sergei I. Ivlev, Eric Meggers

TL;DR
Scientists designed a new ligand that creates a stable chiral iron complex for enantioselective catalysis, using an achiral starting material.
Contribution
First chiral-at-iron catalyst derived from an achiral tetradentate ligand for asymmetric catalysis.
Findings
A linear tetradentate NCCN ligand was synthesized with two mesoionic carbene donors.
The iron complex showed configurational stability and enantioselective catalytic activity in C(sp3)−H amination and Cannizzaro reactions.
Abstract
Ligand design plays a crucial role in developing chiral transition metal complexes with enhanced or new catalytic properties. Here, we report our progress toward a new class of linear tetradentate NCCN ligands incorporating strongly σ‐donating carbene moieties. The NCCN ligand coordinates to iron(II) in a cis‐α topology, with two pyridine donors occupying the apical positions and two 1,2,3‐triazolin‐5‐ylidene mesoionic carbene (MIC) donors in the equatorial plane. Two acetonitrile ligands complete the octahedral coordination sphere, and their lability provides the basis for the observed catalytic activity. Notably, the two strongly σ‐donating MIC groups create a strong ligand field, which is critical for achieving configurational stability of the metal‐centered stereogenicity. This design strategy thus enabled the first chiral‐at‐iron catalyst derived from an achiral tetradentate…
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Taxonomy
TopicsN-Heterocyclic Carbenes in Organic and Inorganic Chemistry · Asymmetric Hydrogenation and Catalysis · Organometallic Complex Synthesis and Catalysis
