Monodentate σ-Accepting Boron-Based Ligands Bearing Square-Planar Ni(0) Centers

Transition metals are known to work as electron donors toward electron-accepting heavier-group-13 elements (Al, Ga, and In), called Z-type ligands. However, complexes with boron-based Z-type ligands are stable only in the presence of additional coordination units (the so-called "supported-ligand" strategy). Here, we report the synthesis and characterization of square-planar Ni(0) complexes that bear tris(perfluoroaryl)boranes as monodentate Z-type ligands, even though such coordination geometry has been traditionally associated with Ni(II) species based on the well-established ligand-field theory. A combined theoretical and experimental approach revealed a mixed covalent/dative character for the Ni-B bonds. This strategy uses frustrated L/Z-ligand pairs that combine sterically encumbered electron-donating (L-type) and electron-accepting ligands to form noncovalent interactions over L-M-Z units to achieve unprecedented low-valent transition metal species with monodentate Z-type ligands.

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Publication Details

Journal
Journal of the American Chemical Society
Published
2025-02-28
DOI
https://doi.org/10.1021/jacs.4c15892
Citations
5
Primary Topic
Organoboron and organosilicon chemistry
Type
article
Field-Weighted Citation Impact
4.68

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article

Monodentate σ-Accepting Boron-Based Ligands Bearing Square-Planar Ni(0) Centers

Sensuke Ogoshi, Takahiro Kawakita, Yoichi Hoshimoto, Yasuhiro Yamauchi et al.
5 citations
Journal of the American Chemical Society
Organoboron and organosilicon chemistry
4.68
article

Monodentate σ-Accepting Boron-Based Ligands Bearing Square-Planar Ni(0) Centers

Sensuke Ogoshi, Takahiro Kawakita, Yoichi Hoshimoto, Yasuhiro Yamauchi, Yuta Uetake, Hidehiro Sakurai, Yasuo Takeichi, Yutaka Mondori
article en
5 citations

Abstract

Transition metals are known to work as electron donors toward electron-accepting heavier-group-13 elements (Al, Ga, and In), called Z-type ligands. However, complexes with boron-based Z-type ligands are stable only in the presence of additional coordination units (the so-called "supported-ligand" strategy). Here, we report the synthesis and characterization of square-planar Ni(0) complexes that bear tris(perfluoroaryl)boranes as monodentate Z-type ligands, even though such coordination geometry has been traditionally associated with Ni(II) species based on the well-established ligand-field theory. A combined theoretical and experimental approach revealed a mixed covalent/dative character for the Ni-B bonds. This strategy uses frustrated L/Z-ligand pairs that combine sterically encumbered electron-donating (L-type) and electron-accepting ligands to form noncovalent interactions over L-M-Z units to achieve unprecedented low-valent transition metal species with monodentate Z-type ligands.

Journal of the American Chemical SocietyVol. 147(10)
Applied Science Private University (JO), Faculty (United Kingdom) (GB), Center for Research and Interdisciplinarity (FR), Graduate School USA (US), The University of Osaka (JP)
Japan Society for the Promotion of Science, Fusion Oriented REsearch for disruptive Science and Technology
Openalex Percentile: Top 6%
Organoboron and organosilicon chemistry
4.68
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