Ambient Temperature Isolation of a Monatomic Boron(0) Complex

The first bottleable example of a neutral Group 13 atom bound only by neutral donor ligands (L) has been fully characterized by spectroscopic methods and its structure determined by a single-crystal X-ray diffraction study. A two-coordinate paramagnetic L<sub>2</sub>B<sup>0</sup> complex can readily be accessed through a facile reduction reaction and is stabilized by π-accepting cyclic (alkyl)(amino)carbene (CAAC) ligands. Further reduction of (CAAC)<sub>2</sub>B leads to the isolation of a stable diamagnetic boride anion. In turn, oxidation leads to the putative formation of a transient two-coordinate cationic borylene, which has been trapped to form a stable boron(I) complex. Density functional theory calculations support the formulation of (CAAC)<sub>2</sub>B as a boron(0) complex stabilized by strong multiple bonding.

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Publication Details

Journal
Journal of the American Chemical Society
Published
2025-01-16
DOI
https://doi.org/10.1021/jacs.4c14915
Citations
7
Primary Topic
Organoboron and organosilicon chemistry
Type
article
Field-Weighted Citation Impact
6.55

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article

Ambient Temperature Isolation of a Monatomic Boron(0) Complex

William Kennedy, Vignesh Pattathil, Yuxiang Wei, Felipe Fantuzzi et al.
7 citations
Journal of the American Chemical Society
Organoboron and organosilicon chemistry
6.55
article

Ambient Temperature Isolation of a Monatomic Boron(0) Complex

William Kennedy, Vignesh Pattathil, Yuxiang Wei, Felipe Fantuzzi, Conor Pranckevicius
article en
7 citations

Abstract

The first bottleable example of a neutral Group 13 atom bound only by neutral donor ligands (L) has been fully characterized by spectroscopic methods and its structure determined by a single-crystal X-ray diffraction study. A two-coordinate paramagnetic L<sub>2</sub>B<sup>0</sup> complex can readily be accessed through a facile reduction reaction and is stabilized by π-accepting cyclic (alkyl)(amino)carbene (CAAC) ligands. Further reduction of (CAAC)<sub>2</sub>B leads to the isolation of a stable diamagnetic boride anion. In turn, oxidation leads to the putative formation of a transient two-coordinate cationic borylene, which has been trapped to form a stable boron(I) complex. Density functional theory calculations support the formulation of (CAAC)<sub>2</sub>B as a boron(0) complex stabilized by strong multiple bonding.

Journal of the American Chemical SocietyVol. 147(4)
University of British Columbia (CA), University of Kent (GB), Okanagan University College (CA)
Canada Foundation for Innovation, European Cooperation in Science and Technology, Natural Sciences and Engineering Research Council of Canada
Clean water and sanitation
Openalex Percentile: Top 4%
Organoboron and organosilicon chemistry
6.55
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