Sea-shell-like B31+and B32: two new axially chiral members of the borospherene family

• Published in: RSC Advances Vol. 10; no. 17; pp. 10129 - 10133
• Main Authors: Pei, Ling, Yan, Miao, Zhao, Xiao-Yun, Mu, Yue-Wen, Lu, Hai-Gang, Wu, Yan-Bo, Li, Si-Dian
• Format: Journal Article
• Language: English
• Published: Cambridge Royal Society of Chemistry (RSC) 10.03.2020; Royal Society of Chemistry; The Royal Society of Chemistry
• Subjects: Aromaticity; Boron; Cages; Chemistry; Computer simulation; Covalent bonds; Equivalence; First principles; Fullerenes; Molecular dynamics; Raman spectroscopy; simulation models; ultraviolet-visible spectroscopy
• ISSN: 2046-2069; 2046-2069
• DOI: 10.1039/d0ra01087a

Since the discovery of the cage-like borospherenes D2d B40−/0 and the first axially chiral borospherenes C3/C2 B39−, a series of fullerene-like boron clusters in different charge states have been reported in theory. Based on extensive global minimum searches and first-principles theory calculations, we present herein two new axially chiral members C2 B31+ (I) and C2 B32 (VI) to the borospherene family. B31+ (I) features two equivalent heptagons on the top and one octagon at the bottom on the cage surface, while B32 (VI) possesses two equivalent heptagons on top and two equivalent heptagons at the bottom. Detailed bonding analyses show that both sea-shell-like B31+ (I) and B32 (VI) follow the universal σ + π double delocalization bonding pattern of the borospherene family, with ten delocalized π bonds over a σ skeleton, rendering spherical aromaticity to the systems. Extensive molecular dynamics simulations show that these novel borospherenes are kinetically stable below 1000 K. The IR, Raman, and UV-vis spectra of B31+ (I) and B32 (VI) are computationally simulated to facilitate their future experimental characterizations.