High-ResolutionPhotoelectron Imaging of Cryogenically-CooledB<sub>8</sub><sup>–</sup> and CB<sub>7</sub><sup>–</sup> Clusters: From Borozene to Carborozene

The closed-shell B<sub>7</sub><sup>3–</sup>, B<sub>8</sub><sup>2–</sup>, and B<sub>9</sub><sup>–</sup> species are recognized recently to be electron-precise molecular wheels with three delocalized π-bonds reminiscent of benzene, giving rise to the concept of “borozene”. The B<sub>8</sub><sup>2–</sup> borozene is especially stable because the B<sub>7</sub> ring has the right size to host a central boron atom. Replacing a B atom by C yields a highly stable closed-shell CB<sub>7</sub><sup>–</sup>, which is isoelectronic to B<sub>8</sub><sup>2–</sup>. Here we use high-resolution cryogenic photoelectron imaging to probe B<sub>8</sub><sup>–</sup> and CB<sub>7</sub><sup>–</sup>, revealing rich vibrational information about B<sub>8</sub> and CB<sub>7</sub> and the vibrational modes responsible for the structure changes from the anions to the neutrals. Surprisingly, a minor isomer is also observed for B<sub>8</sub><sup>–</sup> and found to be due to Jahn–Teller splitting, analogous to the Jahn–Teller effect in the C<sub>6</sub>H<sub>6</sub><sup>+</sup> benzene cation. The transformation from the B<sub>8</sub><sup>2–</sup> borozene to the CB<sub>7</sub><sup>–</sup> carborozene is similar to that from the B<sub>12</sub>H<sub>12</sub><sup>2–</sup> borane to the CB<sub>11</sub>H<sub>12</sub><sup>–</sup> carborane.

Publication Details

Journal
Figshare
Published
2025-02-19
DOI
https://doi.org/10.1021/acs.jpclett.5c00208.s001
Primary Topic
Boron and Carbon Nanomaterials Research
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article
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article

High-ResolutionPhotoelectron Imaging of Cryogenically-CooledB8– and CB7– Clusters: From Borozene to Carborozene

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Boron and Carbon Nanomaterials Research
article

High-ResolutionPhotoelectron Imaging of Cryogenically-CooledB8– and CB7– Clusters: From Borozene to Carborozene

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Abstract

The closed-shell B<sub>7</sub><sup>3–</sup>, B<sub>8</sub><sup>2–</sup>, and B<sub>9</sub><sup>–</sup> species are recognized recently to be electron-precise molecular wheels with three delocalized π-bonds reminiscent of benzene, giving rise to the concept of “borozene”. The B<sub>8</sub><sup>2–</sup> borozene is especially stable because the B<sub>7</sub> ring has the right size to host a central boron atom. Replacing a B atom by C yields a highly stable closed-shell CB<sub>7</sub><sup>–</sup>, which is isoelectronic to B<sub>8</sub><sup>2–</sup>. Here we use high-resolution cryogenic photoelectron imaging to probe B<sub>8</sub><sup>–</sup> and CB<sub>7</sub><sup>–</sup>, revealing rich vibrational information about B<sub>8</sub> and CB<sub>7</sub> and the vibrational modes responsible for the structure changes from the anions to the neutrals. Surprisingly, a minor isomer is also observed for B<sub>8</sub><sup>–</sup> and found to be due to Jahn–Teller splitting, analogous to the Jahn–Teller effect in the C<sub>6</sub>H<sub>6</sub><sup>+</sup> benzene cation. The transformation from the B<sub>8</sub><sup>2–</sup> borozene to the CB<sub>7</sub><sup>–</sup> carborozene is similar to that from the B<sub>12</sub>H<sub>12</sub><sup>2–</sup> borane to the CB<sub>11</sub>H<sub>12</sub><sup>–</sup> carborane.

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Boron and Carbon Nanomaterials Research
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