Preparation and Reactivity of Anionic Iron Sandwich Complex Bearing π‐Phenol Ligand Acting as Proton‐Coupled Electron Transfer Reagent

A neutral Fe(II) sandwich complex bearing a π-phenol ligand with a trifluoroborate substituent [Cp*Fe(η<sup>6</sup>-2-<sup>t</sup>Bu-6-BF<sub>3</sub>-C<sub>6</sub>H<sub>3</sub>OH)] is designed and prepared, which affords the corresponding anionic Fe(I) sandwich complex [Cp*Fe(η<sup>6</sup>-2-<sup>t</sup>Bu-6-BF<sub>3</sub>-C<sub>6</sub>H<sub>3</sub>OH)]<sup>-</sup> with an effective O-H bond dissociation free energy at 40.7 kcal/mol in tetrahydrofuran on treatment with KC<sub>8</sub>. The anionic complex acts as a proton-coupled electron transfer reagent for the reduction of organic substrates such as acetophenone and anthracene, whereas the reaction with a Mo(IV) nitride complex leads to the stoichiometric formation of ammonia.

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Publication Details

Journal
Chemistry - An Asian Journal
Published
2025-12-04
DOI
https://doi.org/10.1002/asia.202500951
Citations
1
Primary Topic
Metal-Catalyzed Oxygenation Mechanisms
Type
article
Field-Weighted Citation Impact
0.54

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article

Preparation and Reactivity of Anionic Iron Sandwich Complex Bearing π‐Phenol Ligand Acting as Proton‐Coupled Electron Transfer Reagent

Soma Yamamoto, Yoshiaki Nishibayashi, Yoshiaki Tanabe, Shogo Kuriyama
1 citations
Chemistry - An Asian Journal
Metal-Catalyzed Oxygenation Mechanisms
0.54
article

Preparation and Reactivity of Anionic Iron Sandwich Complex Bearing π‐Phenol Ligand Acting as Proton‐Coupled Electron Transfer Reagent

Soma Yamamoto, Yoshiaki Nishibayashi, Yoshiaki Tanabe, Shogo Kuriyama
article en
1 citations

Abstract

A neutral Fe(II) sandwich complex bearing a π-phenol ligand with a trifluoroborate substituent [Cp*Fe(η<sup>6</sup>-2-<sup>t</sup>Bu-6-BF<sub>3</sub>-C<sub>6</sub>H<sub>3</sub>OH)] is designed and prepared, which affords the corresponding anionic Fe(I) sandwich complex [Cp*Fe(η<sup>6</sup>-2-<sup>t</sup>Bu-6-BF<sub>3</sub>-C<sub>6</sub>H<sub>3</sub>OH)]<sup>-</sup> with an effective O-H bond dissociation free energy at 40.7 kcal/mol in tetrahydrofuran on treatment with KC<sub>8</sub>. The anionic complex acts as a proton-coupled electron transfer reagent for the reduction of organic substrates such as acetophenone and anthracene, whereas the reaction with a Mo(IV) nitride complex leads to the stoichiometric formation of ammonia.

Chemistry - An Asian JournalVol. 21(1)
The University of Tokyo (JP)
Ministry of Education, Culture, Sports, Science and Technology, Japan Society for the Promotion of Science
Openalex Percentile: Top 28%
Metal-Catalyzed Oxygenation Mechanisms
0.54
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