Ruthenium Complexes Bearing a Tetradentate Hemilabile Ligand: Synthesis, Structure, Hemilabile Feature, and Catalytic Application to C–H Borylation of Unactivated Arenes

Ruthenium complexes bearing a rationally designed tetradentate hemilabile ligand have been developed. The structures of the complexes and the hemilabile feature of the ligand have been disclosed by X-ray crystallography and NMR analyses. Moreover, in a ruthenium-catalyzed C(sp2)–H borylation of unactivated arenes, such a type of complex was found to show superior catalytic reactivity compared to tetradentate or tridentate phosphine ligands, which suggested that the hemilabile feature of the ligand is the key factor in promoting the reaction efficiently.

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Publication Details

Journal
Organometallics
Published
2024-12-23
DOI
https://doi.org/10.1021/acs.organomet.4c00424
Citations
1
Primary Topic
Asymmetric Hydrogenation and Catalysis
Type
article
Field-Weighted Citation Impact
0.16

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article

Ruthenium Complexes Bearing a Tetradentate Hemilabile Ligand: Synthesis, Structure, Hemilabile Feature, and Catalytic Application to C–H Borylation of Unactivated Arenes

Kohei Takahashi, Yumeng Liao, Nobuharu Iwasawa
1 citations
Organometallics
Asymmetric Hydrogenation and Catalysis
0.16
article

Ruthenium Complexes Bearing a Tetradentate Hemilabile Ligand: Synthesis, Structure, Hemilabile Feature, and Catalytic Application to C–H Borylation of Unactivated Arenes

Kohei Takahashi, Yumeng Liao, Nobuharu Iwasawa
article en
1 citations

Abstract

Ruthenium complexes bearing a rationally designed tetradentate hemilabile ligand have been developed. The structures of the complexes and the hemilabile feature of the ligand have been disclosed by X-ray crystallography and NMR analyses. Moreover, in a ruthenium-catalyzed C(sp2)–H borylation of unactivated arenes, such a type of complex was found to show superior catalytic reactivity compared to tetradentate or tridentate phosphine ligands, which suggested that the hemilabile feature of the ligand is the key factor in promoting the reaction efficiently.

OrganometallicsVol. 44(1)
Tokyo Institute of Technology (JP)
Japan Society for the Promotion of Science
Openalex Percentile: Top 55%
Asymmetric Hydrogenation and Catalysis
0.16
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