Rearrangement of dicarboranyl methyl cation to icosahedral C3 B9 H12 + : An ab initio dynamics view
Status PubMed-not-MEDLINE Jazyk angličtina Země Spojené státy americké Médium print-electronic
Typ dokumentu časopisecké články
Grantová podpora
22-03945S
Czech Science Foundation
Science and Engineering Research Board, Year of Science Chair
PubMed
35612818
DOI
10.1002/jcc.26880
Knihovny.cz E-zdroje
- Klíčová slova
- carborane cation, carboranes, metadynamics, tropylium rearrangement,
- Publikační typ
- časopisecké články MeSH
Closo-carborane anions are prominent, whereas the cations of the same are less abundant in the literature. As these ions have similar size and are weakly coordinating, the ionic liquids of these two ions could have important applications in many areas of chemistry. In view of limited number of polyhedral carborane cations available, we revisited the rearrangement of dicarboranyl methyl cation (7-CH2 7,9-nido-C2 B9 H10 + ) using ab initio molecular dynamics calculations with metadynamics. Our simulations confirmed the concerted mechanism of the rearrangement. We believe this work will resume the interest in its synthesis and carborane cations in general.
Department of Chemistry Boston University Boston Massachusetts USA
Department of Inorganic and Physical Chemistry Indian Institute of Science Bangalore India
Institute of Inorganic Chemistry Czech Academy of Sciences Husinec Řež Czech Republic
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