Discovery of bicyclic borane molecule B14H26

The discovery of fullerene following the synthesis of graphene marked a paradigm shift in chemistry. Here, we report the discovery of biycycloborane, arising from the synthesis of borophane (hydrogen boride). Uniquely, this synthesis method involves a decomposition mechanism rather than traditional atom-by-atom assembly, marking an unique approach to constructing complex borane structures. The mass spectrometry unveiled that the stable molecule has a mass of 178 in atomic mass unit with a stoichiometry of B<sub>14</sub>H<sub>26</sub>. Optical spectra and simulations further evidenced its bicyclic structure, featuring fulvene-like heptagons or octagons. This borane molecule, analogous to cyclic hydrocarbons, adopts a unit configuration with a three-center two-electron (3c-2e) bonding, akin to diborane. The B<sub>14</sub>H<sub>26</sub> molecule has been historically anticipated as a distant descendant of the dodecahedron borane, but it was born from the hydrogen boride sheet with a non-symmorphic symmetry. The discovery of biycycloborane expands the frontiers of boron chemistry, promising advancements in boron-based nanomaterials and beyond.

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Publication Details

Journal
Communications Chemistry
Published
2025-01-16
DOI
https://doi.org/10.1038/s42004-025-01409-1
Primary Topic
Boron Compounds in Chemistry
Type
article
Field-Weighted Citation Impact
0.00

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article

Discovery of bicyclic borane molecule B14H26

Jun Yoshinobu, Yasunobu Ando, Iwao Matsuda, Tomoko Fujino et al.
Communications Chemistry
Boron Compounds in Chemistry
article

Discovery of bicyclic borane molecule B14H26

Jun Yoshinobu, Yasunobu Ando, Iwao Matsuda, Tomoko Fujino, Yuki Tsujikawa, Takeru Nakashima, Hatsumi Mori, Masafumi Horio, Xiaoni Zhang, Takahiro Kondo, Tianle Wang, Kazuki Yamaguchi, Haruto Sakurai
article en

Abstract

The discovery of fullerene following the synthesis of graphene marked a paradigm shift in chemistry. Here, we report the discovery of biycycloborane, arising from the synthesis of borophane (hydrogen boride). Uniquely, this synthesis method involves a decomposition mechanism rather than traditional atom-by-atom assembly, marking an unique approach to constructing complex borane structures. The mass spectrometry unveiled that the stable molecule has a mass of 178 in atomic mass unit with a stoichiometry of B<sub>14</sub>H<sub>26</sub>. Optical spectra and simulations further evidenced its bicyclic structure, featuring fulvene-like heptagons or octagons. This borane molecule, analogous to cyclic hydrocarbons, adopts a unit configuration with a three-center two-electron (3c-2e) bonding, akin to diborane. The B<sub>14</sub>H<sub>26</sub> molecule has been historically anticipated as a distant descendant of the dodecahedron borane, but it was born from the hydrogen boride sheet with a non-symmorphic symmetry. The discovery of biycycloborane expands the frontiers of boron chemistry, promising advancements in boron-based nanomaterials and beyond.

Communications ChemistryVol. 8(1)
Tokyo Institute of Technology (JP), University of Tsukuba (JP), The University of Tokyo (JP)
Japan Society for the Promotion of Science, Core Research for Evolutional Science and Technology
Openalex Percentile: Top 99%
Boron Compounds in Chemistry
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