| Autor: |
Barthélemy, Antoine, Scherer, Harald, Daub, Michael, Bugnet, Alexis, Krossing, Ingo |
| Předmět: |
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| Zdroj: |
Angewandte Chemie International Edition; 11/20/2023, Vol. 62 Issue 47, p1-9, 9p |
| Abstrakt: |
The reaction of bisdicyclohexylphosphinoethane (dcpe) and the subvalent MI sources [MI(PhF)2][pf] (M=Ga+, In+; [pf]−=[Al(ORF)4]−; RF=C(CF3)3) yielded the salts [{M(dcpe)}2][pf]2, containing the first dicationic, trans‐bent digallene and diindene structures reported so far. The non‐classical MI⇆MI double bonds are surprisingly short and display a ditetrylene‐like structure. The bonding situation was extensively analyzed by quantum chemical calculations, QTAIM (Quantum Theory of Atoms in Molecules) and EDA‐NOCV (Energy Decomposition Analysis with the combination of Natural Orbitals for Chemical Valence) analyses and is compared to that in the isoelectronic and isostructural, but neutral digermenes and distannenes. The dissolved [{Ga(dcpe)}2]2+([pf]−)2 readily reacts with 1‐hexene, cyclooctyne, diphenyldisulfide, diphenylphosphine and under mild conditions at room temperature. This reactivity is analyzed and rationalized. [ABSTRACT FROM AUTHOR] |
| Databáze: |
Complementary Index |
| Externí odkaz: |
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