Abstract

Singlet carbenes are extensively studied compounds capable of electrophilic, nucleophilic or ambiphillic behaviour. The ambiphilic reactivity of singlet carbenes have been conventionally observed in orthogonal planes. Here, we report a detailed bonding and reactivity study of a homobimetallic carbon complex [(MCp*)2(μ-NPh)(μ-C)] (1M, M = Fe, Ru, Os) that shows ambiphilicity in the same direction. The structure of this complex can be considered as two fused three-membered M-C-M and M-N-M rings. The bonding analysis suggests that these 17VE homobimetallic complexes have one formal M-M bond with a bridging carbene centre featuring a high lying spn-hybridised lone pair. Accordingly, the carbene centre shows high proton affinity and act as a good 2e- donor to Lewis acids and transition metal fragment. Apart from the transition metal non-bonding electrons, the π-framework of M-C-M and M-N-M arms can be best described as 3c-2e- bonds. The two transition metals in the four-membered skeleton generate many low-lying, virtual orbitals. These low-lying virtual orbitals induces electron excitation from the spn-hybrid orbital in presence of H- and other 2e- donor ligands such as PMe3, NHC and CO. Hence, the spn-hybrid lone pair orbital shows σ-hole reactivity in presence of Lewis bases.

Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call