Exploring the Effect of Pincer Rigidity on Oxidative Addition Reactions with Cobalt(I) Complexes

Cobalt complexes containing the 2,6-diaminopyridinesubstituted PNP pincer (iPrPNMeNP = 2,6-(iPr2PNMe)2(C5H3N)) were synthesized. A combination of solid-state structures and investigation of the cobalt(I)/(II) redox potentials established a relatively rigid and electron-donating chelating ligand as compared to iPrPNP (iPrPNP = 2,6(iPr2PCH2)2(C5H3N)). Based on a buried volume analysis, the two pincer ligands are sterically indistinguishable. Nearly planar, diamagnetic, four-coordinate complexes were observed independent of the field strength (chloride, alkyl, aryl) of the fourth ligand completing the coordination sphere of the metal. Computational studies supported a higher barrier for C-H oxidative addition, largely a result of the increased rigidity of the pincer. The increased oxidative addition barrier resulted in stabilization of (iPrPNMeNP)Co(I) complexes, enabling the characterization of the cobalt boryl and the cobalt hydride dimer by X-ray crystallography. Moreover, (iPrPNMeNP)CoMe served as an efficient precatalyst for alkene hydroboration likely because of the reduced propensity to undergo oxidative addition, demonstrating that reactivity and catalytic performance can be tuned by rigidity of pincer ligands.

Automated summary

Cobalt complexes with 2,6-diaminopyridinesubstituted PNP pincer ligand were synthesized and studied. The PNP pincer ligand showed higher rigidity and electron-donating properties compared to the iPrPNP ligand. The coordination sphere of the metal was completed by a fourth ligand, resulting in planar, diamagnetic, four-coordinate complexes. Computational studies indicated that the increased rigidity of the pincer ligand led to a higher barrier for C-H oxidative addition. The reduced reactivity of (iPrPNMeNP)CoMe enabled it to be an efficient precatalyst for alkene hydroboration.