Coordination-induced axial chirality controls the metal-centred configuration in a stereogenic-at-iron catalyst

A new approach is introduced to control the metal-centred configuration of stereogenic-at-iron catalysts by utilizing axial ligand chirality, which becomes locked upon metal coordination. This strategy is applied to an iron catalyst containing two chelating <i>N</i>-(2-pyridyl)-substituted triazol-5-ylidene mesoionic carbenes (MICs) resulting in a helical topology with a stereogenic iron centre.

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Publication Details

Journal
Chemical Communications
Published
2025-01-01
DOI
https://doi.org/10.1039/d4cc06227b
Citations
1
Primary Topic
Axial and Atropisomeric Chirality Synthesis
Type
article
Field-Weighted Citation Impact
0.94

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Coordination-induced axial chirality controls the metal-centred configuration in a stereogenic-at-iron catalyst

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Chemical Communications
Axial and Atropisomeric Chirality Synthesis
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article

Coordination-induced axial chirality controls the metal-centred configuration in a stereogenic-at-iron catalyst

Sergei I. Ivlev, Nemrud Demirel, Eric Meggers, Xiulan Xie, Benedikt Buchberger
article en
1 citations

Abstract

A new approach is introduced to control the metal-centred configuration of stereogenic-at-iron catalysts by utilizing axial ligand chirality, which becomes locked upon metal coordination. This strategy is applied to an iron catalyst containing two chelating <i>N</i>-(2-pyridyl)-substituted triazol-5-ylidene mesoionic carbenes (MICs) resulting in a helical topology with a stereogenic iron centre.

Chemical CommunicationsVol. 61(9)
Philipps University of Marburg (DE)
H2020 European Research Council
Openalex Percentile: Top 30%
Axial and Atropisomeric Chirality Synthesis
0.94
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