C(spn)−X (n=1–3) Bond Activation by Palladium

• Published in: Chemistry : a European journal 2022-05, Vol.28 (26), p.e202103953-n/a
• Main Authors: Hansen, Thomas, Sun, Xiaobo, Dalla Tiezza, Marco, Zeist, Willem‐Jan, Poater, Jordi, Hamlin, Trevor A., Bickelhaupt, F. M.
• Format: Article
• Language: English
• Subjects: activation strain model; Bonding strength; Catalysts; Chemistry; Coordination numbers; density functional calculations; Density functional theory; homogeneous catalysis; oxidative addition; Palladium; reactivity; Relativistic theory; Substrates
• ISSN: 0947-6539; 1521-3765; 1521-3765
• DOI: 10.1002/chem.202103953

We have studied the palladium‐mediated activation of C(spn)−X bonds (n = 1–3 and X = H, CH3, Cl) in archetypal model substrates H3C−CH2−X, H2C=CH−X and HC≡C−X by catalysts PdLn with Ln = no ligand, Cl−, and (PH3)2, using relativistic density functional theory at ZORA‐BLYP/TZ2P. The oxidative addition barrier decreases along this series, even though the strength of the bonds increases going from C(sp3)−X, to C(sp2)−X, to C(sp)−X. Activation strain and matching energy decomposition analyses reveal that the decreased oxidative addition barrier going from sp3, to sp2, to sp, originates from a reduction in the destabilizing steric (Pauli) repulsion between catalyst and substrate. This is the direct consequence of the decreasing coordination number of the carbon atom in C(spn)−X, which goes from four, to three, to two along this series. The associated net stabilization of the catalyst–substrate interaction dominates the trend in strain energy which indeed becomes more destabilizing along this same series as the bond becomes stronger from C(sp3)−X to C(sp)−X. Less is more! Our quantum chemical analyses reveal that the activity of palladium catalysts towards C−X bond activation increases along ethane, ethylene, acetylene because the steric repulsion between catalyst and substrate is relieved as the number of substituents around the carbon atom goes down.