Intramolecular C–N bond activation by a transient boryl anion
Emily E. Nahon,
Gareth R. Nelmes,
Penelope J. Brothers
et al.
Abstract:Electrophilic or nucleophilic? Reduction of a bulky boron bromide with lithium leads to C–N bond cleavage though a nucleophilic boryl anion. In contrast, reaction with an anionic iron carbonyl salt leads to cooperative reduction of CO.
“…4). The compound is isostructural to the boron analogue recently reported by us 26 and similar to the benzylidynebridged diiron complex previously reported by Sitzmann and co-workers. 27 It can be envisioned that [{( Dipp NON)AlOC(µ-FeCp)} 2 ] may be formed from the iron aluminyl complex ( Dipp NON)AlFp, by simple loss of a carbonyl ligand from each iron centre and dimerisation.…”
“…Nucleophilic reactivity of the [Fp] − carbonyl ligands has been previously reported, 28 and a similar mechanism was proposed for the boron analogue. 26…”
“…4). The compound is isostructural to the boron analogue recently reported by us 26 and similar to the benzylidynebridged diiron complex previously reported by Sitzmann and co-workers. 27 It can be envisioned that [{( Dipp NON)AlOC(µ-FeCp)} 2 ] may be formed from the iron aluminyl complex ( Dipp NON)AlFp, by simple loss of a carbonyl ligand from each iron centre and dimerisation.…”
“…Nucleophilic reactivity of the [Fp] − carbonyl ligands has been previously reported, 28 and a similar mechanism was proposed for the boron analogue. 26…”
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.