Diverse and Selective Metal–Ligand Cooperative Routes for Activating Non-Functionalized Ketones

The rhodium and iridium complexes [Cp*M­(κ3N,N′,N″-L)]­[SbF6] (Cp* = η5-C5Me5; M = Rh, 1; Ir, 2; HL = pyridinyl-amidine ligand) exhibit three different
cooperative
metal–ligand reactivity modes when interacting with nonfunctionalized
ketones. With the methyl ketones CH3COR (R = CH3, Ph, CF3), activation of the ketone methyl C­(sp3)–H bond yields ketonyl compounds of formula [Cp*M­(CH2COR)­(κ2N,N′-HL)]­[SbF6]. With the ketones (CF3)2CO and CF3COPh, the complexes add to the
CO double bond of the ketone. The addition of the iridium
compound 2 occurs across the metal atom and the exocyclic
carbon of the dearomatized pyridinyl moiety, and that of the rhodium
analogue 1 takes place through the rhodium atom and the
exocyclic methylene carbon of the Cp* ligand of the intermediate fulvene
complex. In the rhodium case, the resulting metal-alkoxide derivative
evolves to give rise to rhodium derivatives containing up to four
added ketone molecules. In all of these processes, no additives are
required, rendering them atom 100% efficient procedures for bond activation.
From a mechanistic point of view, DFT calculation reveals that the
diverse and selective behavior of 1 and 2 toward ketones can be explained by invoking three different intermediates,
each driving the process through distinct reaction pathways.