2023•Journal of the American Chemical SocietyOpen access

Planar Four-Membered Diboron Actinide Compound with Double Möbius Aromaticity

Xuhui Lin, Wei Wu, Yirong Mo

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Abstract

High Resolution Image Download MS PowerPoint Slide The Möbius rule predicts that a planar four-membered metallacycle can be aromatic with four mobile electrons, but such a simple ring has escaped recognition because it usually favors Hückel anti-aromaticity. Here, we report that a quasi-square four-membered actinide compound (Pa 2 B 2 ) is doubly Möbius aromatic. Chemical bonding analyses reveal that this diboron protactinium molecule has four delocalized π electrons in addition to four delocalized σ electrons, satisfying the 4n Möbius rule for both σ and π components. Energetically, the block-localized wavefunction method, which is the simplest variant of ab initio valence bond theory, shows that the delocalization energy for the π and σ electrons reaches up to 65.0 and 72.3 kcal/mol, respectively, while the extra cyclic resonance energy (ECRE) amounts to 45 kcal/mol. The large positive ECRE values strongly confirm the unprecedented double Möbius aromaticity in Pa 2 B 2 . We anticipate that this new type of aromatic molecule can enrich the concept of Möbius aromaticity and open a new avenue for actinide compounds.

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High Resolution Image Download MS PowerPoint Slide The Möbius rule predicts that a planar four-membered metallacycle can be aromatic with four mobile electrons, but such a simple ring has escaped recognition because it usually favors Hückel anti-aromaticity. Here, we report that a quasi-square four-membered actinide compound (Pa 2 B 2 ) is doubly Möbius aromatic. Chemical bonding analyses reveal that this diboron protactinium molecule has four delocalized π electrons in addition to four delocalized σ electrons, satisfying the 4n Möbius rule for both σ and π components. Energetically, the block-localized wavefunction method, which is the simplest variant of ab initio valence bond theory, shows that the delocalization energy for the π and σ electrons reaches up to 65.0 and 72.3 kcal/mol, respectively, while the extra cyclic resonance energy (ECRE) amounts to 45 kcal/mol. The large positive ECRE values strongly confirm the unprecedented double Möbius aromaticity in Pa 2 B 2 . We anticipate that this new type of aromatic molecule can enrich the concept of Möbius aromaticity and open a new avenue for actinide compounds.

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Available abstract

High Resolution Image Download MS PowerPoint Slide The Möbius rule predicts that a planar four-membered metallacycle can be aromatic with four mobile electrons, but such a simple ring has escaped recognition because it usually favors Hückel anti-aromaticity. Here, we report that a quasi-square four-membered actinide compound (Pa 2 B 2 ) is doubly Möbius aromatic. Chemical bonding analyses reveal that this diboron protactinium molecule has four delocalized π electrons in addition to four delocalized σ electrons, satisfying the 4n Möbius rule for both σ and π components. Energetically, the block-localized wavefunction method, which is the simplest variant of ab initio valence bond theory, shows that the delocalization energy for the π and σ electrons reaches up to 65.0 and 72.3 kcal/mol, respectively, while the extra cyclic resonance energy (ECRE) amounts to 45 kcal/mol. The large positive ECRE values strongly confirm the unprecedented double Möbius aromaticity in Pa 2 B 2 . We anticipate that this new type of aromatic molecule can enrich the concept of Möbius aromaticity and open a new avenue for actinide compounds.

Key concepts: Aromaticity, Delocalized electron, Chemistry, Computational chemistry, Molecule, Chemical shift, Crystallography, Electron

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