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.
Authors
- William Tiznado (ORCID: https://orcid.org/0000-0002-6061-8879)
- Carlos Cárdenas (ORCID: https://orcid.org/0000-0002-0648-6502)
- Lina María Ruíz (ORCID: https://orcid.org/0000-0002-9363-2730)
- Luis Leyva‐Parra (ORCID: https://orcid.org/0000-0002-4210-1868)
- Williams García-Argote (ORCID: https://orcid.org/0009-0006-6442-8059)
- Rodolfo Pumachagua‐Huertas (ORCID: https://orcid.org/0000-0002-8431-209X)
- Dumer S. Sacanamboy (ORCID: https://orcid.org/0000-0002-3689-3125)
Institutions
- 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)
Publication Details
- Journal
- Molecules
- Published
- 2025-08-31
- DOI
- https://doi.org/10.3390/molecules30173566
- Citations
- 1
- Primary Topic
- Synthesis and Properties of Aromatic Compounds
- Type
- article
- Field-Weighted Citation Impact
- 0.94
Funders
- 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