The variation of coordination modes of aromatic imines in iron carbonyl complexes: Is there a correlation between bond lengths in organometallic model compounds and the reactivity of the ligands in catalytic C–C bond formation reactions?

Abstract

The reaction of aromatic imines with Fe 2(CO) 9 proceeds via a two-step reaction sequence. A C–H activation reaction in ortho-position with respect to the exocyclic imine function is followed by an intramolecular hydrogen transfer reaction towards the former imine carbon atom. The resulting dinuclear iron carbonyl complexes show an aza-ferra-cyclopentadiene ligand which is apically coordinated by the second iron tricarbonyl moiety. Comparing the bond lengths of 43 different compounds, which were synthesized and structurally characterized in our group shows that the iron iron bond length correlates with one of the iron carbon bond lengths. The longer the iron carbon bond between the apically coordinated iron atom and the carbon atom next to the former imine carbon atom is, the shorter is the iron iron bond. The same ligands may be used as the substrates in ruthenium catalyzed C–C bond formation reactions. Whereas most of the imines react via the formal insertion of CO and/or ethylene into the C–H bond in ortho-position to the imine function, the ligands that show the longest iron carbon bond lengths in the model compounds under the same reaction conditions produce different types of isoindolones.