Interpreting Ring Currents from Hückel-Guided σ- and π-Electron Delocalization in Small Boron Rings

The aromaticity of small boron clusters remains under scrutiny due to persistent inconsistencies between magnetic and electronic descriptors. Here, we reexamine B<sub>3</sub><sup>-</sup>, B<sub>3</sub><sup>+</sup>, B<sub>4</sub>, B<sub>4</sub><sup>2+</sup>, and B<sub>4</sub><sup>2-</sup> using a multidimensional approach that integrates Adaptive Natural Density Partitioning, Electron Density of Delocalized Bonds, magnetically induced current density, and the z-component of the induced magnetic field. We introduce a model in which σ-aromaticity arises from two distinct delocalization topologies: a radial 2e<sup>-</sup> σ-pathway and a tangential multicenter circuit formed by alternating filled and vacant sp<sup>2</sup> orbitals. This framework accounts for the evolution of aromaticity upon oxidation or reduction, preserving coherence between electronic structure and magnetic response. B<sub>3</sub><sup>-</sup> features cooperative radial and tangential σ-delocalization, together with a delocalized 2e<sup>-</sup> π-bond, yielding robust double aromaticity. B<sub>3</sub><sup>+</sup> retains σ- and π-aromaticity, but only via a tangential 6e<sup>-</sup> σ-framework, leading to a more compact delocalization and slightly attenuated ring currents. In B<sub>4</sub>, the presence of a radial 2e<sup>-</sup> σ-bond and a 4c-2e π-bond confers partial aromatic character, while the tangential 8e<sup>-</sup> σ-framework satisfies the 4n rule and induces a paratropic current. In contrast, B<sub>4</sub><sup>2+</sup> lacks the radial σ-component but retains a tangential 8e<sup>-</sup> σ-circuit and a 2e<sup>-</sup> 4c-2e π-bond, leading to a σ-antiaromatic and π-aromatic configuration. Finally, B<sub>4</sub><sup>2-</sup>, exhibits delocalized π- and σ-circuits, yielding consistent diatropic ring currents, which confirms its fully doubly aromatic nature. Altogether, this analysis underscores the importance of resolving σ-framework topology and demonstrates that, when radial and tangential contributions are correctly distinguished, Hückel's rule remains a powerful tool for interpreting aromaticity in small boron rings.

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Journal
Molecules
Published
2025-08-31
DOI
https://doi.org/10.3390/molecules30173566
Citations
1
Primary Topic
Synthesis and Properties of Aromatic Compounds
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article
Field-Weighted Citation Impact
0.94

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article

Interpreting Ring Currents from Hückel-Guided σ- and π-Electron Delocalization in Small Boron Rings

William Tiznado, Carlos Cárdenas, Lina María Ruíz, Luis Leyva‐Parra et al.
1 citations
Molecules
Synthesis and Properties of Aromatic Compounds
0.94
article

Interpreting Ring Currents from Hückel-Guided σ- and π-Electron Delocalization in Small Boron Rings

William Tiznado, Carlos Cárdenas, Lina María Ruíz, Luis Leyva‐Parra, Williams García-Argote, Rodolfo Pumachagua‐Huertas, Dumer S. Sacanamboy
article en
1 citations

Abstract

The aromaticity of small boron clusters remains under scrutiny due to persistent inconsistencies between magnetic and electronic descriptors. Here, we reexamine B<sub>3</sub><sup>-</sup>, B<sub>3</sub><sup>+</sup>, B<sub>4</sub>, B<sub>4</sub><sup>2+</sup>, and B<sub>4</sub><sup>2-</sup> using a multidimensional approach that integrates Adaptive Natural Density Partitioning, Electron Density of Delocalized Bonds, magnetically induced current density, and the z-component of the induced magnetic field. We introduce a model in which σ-aromaticity arises from two distinct delocalization topologies: a radial 2e<sup>-</sup> σ-pathway and a tangential multicenter circuit formed by alternating filled and vacant sp<sup>2</sup> orbitals. This framework accounts for the evolution of aromaticity upon oxidation or reduction, preserving coherence between electronic structure and magnetic response. B<sub>3</sub><sup>-</sup> features cooperative radial and tangential σ-delocalization, together with a delocalized 2e<sup>-</sup> π-bond, yielding robust double aromaticity. B<sub>3</sub><sup>+</sup> retains σ- and π-aromaticity, but only via a tangential 6e<sup>-</sup> σ-framework, leading to a more compact delocalization and slightly attenuated ring currents. In B<sub>4</sub>, the presence of a radial 2e<sup>-</sup> σ-bond and a 4c-2e π-bond confers partial aromatic character, while the tangential 8e<sup>-</sup> σ-framework satisfies the 4n rule and induces a paratropic current. In contrast, B<sub>4</sub><sup>2+</sup> lacks the radial σ-component but retains a tangential 8e<sup>-</sup> σ-circuit and a 2e<sup>-</sup> 4c-2e π-bond, leading to a σ-antiaromatic and π-aromatic configuration. Finally, B<sub>4</sub><sup>2-</sup>, exhibits delocalized π- and σ-circuits, yielding consistent diatropic ring currents, which confirms its fully doubly aromatic nature. Altogether, this analysis underscores the importance of resolving σ-framework topology and demonstrates that, when radial and tangential contributions are correctly distinguished, Hückel's rule remains a powerful tool for interpreting aromaticity in small boron rings.

MoleculesVol. 30(17)
Universidad de Santiago de Chile (CL), Federico Villarreal National University (PE), Universidad Andrés Bello (CL), Universidad Autónoma de Chile (CL), Universidad Bernardo O'Higgins (CL), University of Chile (CL)
Agenția Națională pentru Cercetare și Dezvoltare, Universidad Andrés Bello, Agencia Nacional de Investigación y Desarrollo, Centro para el Desarrollo de la Nanociencia y la Nanotecnología, CHIST-ERA
Openalex Percentile: Top 22%
Synthesis and Properties of Aromatic Compounds
0.94
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