Triel Bonds with Methyl Groups as Electron Donors. A Pentacoordinate Carbon Atom.
AIM
Methyl transfer
energy decomposition
substituent effect
Journal
Chemphyschem : a European journal of chemical physics and physical chemistry
ISSN: 1439-7641
Titre abrégé: Chemphyschem
Pays: Germany
ID NLM: 100954211
Informations de publication
Date de publication:
27 Oct 2024
27 Oct 2024
Historique:
revised:
24
10
2024
received:
01
10
2024
accepted:
25
10
2024
medline:
27
10
2024
pubmed:
27
10
2024
entrez:
27
10
2024
Statut:
aheadofprint
Résumé
The triel bond (TrB) formed between Be(CH3)2/Mg(CH3)2 and TrX3 (Tr = B, Al, and Ga; X = H, F, Cl, Br, and I) is investigated via the MP2/aug-cc-pVTZ(PP) quantum chemical protocol. The C atoms of the methyl groups in M(CH3)2 are characterized by a negative electrostatic potential and act as an electron donor in a triel bond with the π-hole above the Tr atom of planar TrX3. The interaction energy spans a wide range between 2 and 69 kcal/mol. Mg(CH3)2 forms a stronger TrB than does Be(CH3)2, which comports with the more negative electrostatic potential on its methyl groups. Some of the complexes involving Mg display a high degree of transfer of the methyl group from Mg to Tr, which is accompanied by an inversion of the bridging methyl and a sizable pyramidalization of the TrX3 unit. The geometries of these complexes have the properties of the long sought pentacoordinate C which has eluded identification and characterization in the past.
Identifiants
pubmed: 39462203
doi: 10.1002/cphc.202400931
doi:
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
e202400931Informations de copyright
© 2024 Wiley‐VCH GmbH.