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φ-Aromaticity in prismatic {Bi$_6$}-based clusters

Peerless, Benjamin 1; Schmidt, Andreas 1; Franzke, Yannick J. J. ; Dehnen, Stefanie 1
1 Institut für Nanotechnologie (INT), Karlsruher Institut für Technologie (KIT)

Abstract:

The occurrence of aromaticity in organic molecules is widely accepted, but its occurrence in purely metallic systems is less widespread. Molecules comprising only metal atoms (M) are known to be able to exhibit aromatic behaviour, sustaining ring currents inside an external magnetic field along M–M connection axes (σ-aromaticity) or above and below the plane (π-aromaticity) for cyclic or cage-type compounds. However, all-metal compounds provide an extension of the electrons’ mobility also in other directions. Here, we show that regular {Bi$_6$} prisms exhibit a non-localizable molecular orbital of f-type symmetry and generate a strong ring current that leads to a behaviour referred to as φ-aromaticity. The experimentally observed heterometallic cluster [{CpRu}$_3$Bi$_6$]–, based on a regular prismatic {Bi$_6$} unit, displays aromatic behaviour; according to quantum chemical calculations, the corresponding hypothetical Bi$_6$$^{2−}$ prism shows a similar behaviour. By contrast, [{(cod)Ir}$_3$Bi$_6$] features a distorted Bi$_6$ moiety that inhibits φ-aromaticity.


Verlagsausgabe §
DOI: 10.5445/IR/1000155363
Veröffentlicht am 30.01.2023
Originalveröffentlichung
DOI: 10.1038/s41557-022-01099-5
Scopus
Zitationen: 16
Dimensions
Zitationen: 20
Cover der Publikation
Zugehörige Institution(en) am KIT Institut für Nanotechnologie (INT)
Publikationstyp Zeitschriftenaufsatz
Publikationsjahr 2022
Sprache Englisch
Identifikator ISSN: 1755-4330, 1755-4349
KITopen-ID: 1000155363
HGF-Programm 43.31.01 (POF IV, LK 01) Multifunctionality Molecular Design & Material Architecture
Erschienen in Nature Chemistry
Verlag Nature Research
Band 15
Heft 3
Seiten 347–356
Vorab online veröffentlicht am 22.12.2022
Schlagwörter Chemical bonding, Density functional theory, Organometallic chemistry, Quantum chemistry
Nachgewiesen in Dimensions
Web of Science
Scopus
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