Mechanistic insights into the α-branched amine formation with pivalic acid assisted C-H bond activation catalysed by Cp*Rh complexes

Density functional theory computations revealed a pivalic acid assisted C-H bond activation mechanism for rhodium catalyzed formation of alpha-branched amines with C-C and C-N bond couplings. The reaction energies of the [Cp*RhCl2](2) dimer and silver cations indicate that the Cp*RhCl+ cation is the active catalyst. The essential role of pivalic acid is a co-catalyst for the activation of the ortho-C(sp(2))-H bond in phenyl(pyrrolidin-1-yl)methanone, while the reaction of NaHCO3 and HCl reduces the overall barrier of the catalytic cycle. In the presence of both pivalic acid and NaHCO3 in the reaction, the C(sp(2))-H bond is activated through a concerted metallation deprotonation process, and the C-C bond coupling is the rate-determining step with a total free energy barrier of 23.9 kcal mol(-1). Without pivalic acid and NaHCO3, the C(sp(2))-H bond can only be activated through a sigma-bond metathesis process and the free energy barrier increases to 32.2 kcal mol(-1). We also investigated the mechanisms of a side reaction for beta-branched amine formation and the reaction without styrene and found that their free energy barriers are 33.4 and 30.5 kcal mol(-1), respectively.

Automated summary

Density functional theory calculations showed that pivalic acid assists in the C-H bond activation mechanism for the formation of alpha-branched amines catalyzed by rhodium. The active catalyst is the Cp*RhCl+ cation. The presence of both pivalic acid and NaHCO3 reduces the overall barrier of the catalytic cycle by facilitating the activation of the ortho-C(sp(2))-H bond in a concerted metallation deprotonation process.