Planar B41- and B42- clusters with double-hexagonal vacancies
Hui Bai1, Teng-Teng Chen2, Qiang Chen3
1Key Laboratory of Coal Science and Technology of Ministry of Education and Shanxi Province, Taiyuan University of Technology, Taiyuan 030024, Shanxi, China and Department of Chemistry, Brown University, Providence, Rhode Island 02912, USA. lai-sheng_wang@brown.edu.
Researchers studied larger boron clusters, B41- and B42-, using photoelectron spectroscopy. They found that quasi-planar structures with double hexagonal vacancies dominate, challenging the persistence of borospherene cages in larger boron systems.
Area of Science:
- Computational Chemistry
- Materials Science
- Spectroscopy
Background:
- Following the discovery of B40 borospherene, interest grew in larger boron clusters.
- A key question is whether borospherene cages persist in larger boron structures.
Purpose of the Study:
- To investigate the structures and bonding of B41- and B42- boron clusters.
- To determine if borospherene cages are stable in these larger clusters.
Main Methods:
- Photoelectron spectroscopy (PES) was employed to study the electronic properties.
- Computational global minimum searches identified low-lying isomers.
- Chemical bonding analyses were performed to understand electronic structure.
Main Results:
- PES spectra for B41- and B42- showed complex features, indicating multiple isomers.
- For B41-, isomer II (double hexagonal vacancy) matched experimental data, with minor single vacancy isomers.
- For B42-, quasi-planar structure VIII (double hexagonal vacancy) was dominant, with other isomers contributing.
- Key isomers of B41- and B42- exhibit π aromaticity, similar to polycyclic aromatic hydrocarbons.
Conclusions:
- Quasi-planar structures with double hexagonal vacancies are favored for B41- and B42-.
- Borospherene cage structures are energetically unfavorable for these larger boron clusters.
- The findings challenge the simple persistence of borospherene cages in larger boron systems.
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