N-substituted aminobiphenyl palladacycles stabilized by dialkylterphenyl phosphanes: Preparation and applications in C-N cross-coupling reactions

Neutral and cationic N-methyl- and N-phenyl-2-aminobiphenyl methanesulfonate palladacycles stabilized with dialkylterphenyl phosphanes have been prepared and characterized. Neutral structures are favored with the less bulky phosphane PMe2ArXyl2, L1, while more sterically demanding ligands PiPr(2)Ar(Xyl2), L3, and PCyp(2)Ar(Xyl2) (Cyp = cyclopentyl), L4, lead to cationic complexes in which the phosphane exhibits a bidentate kappa(1)-P,eta(1)-C-arene coordination mode involving one of the ipso carbon atoms of a flanking terphenyl aryl ring. The complexes were evaluated for activity in C-N cross-coupling reactions and [Pd(N-methyl-2-aminobiphenyl)L4](OMs) (OMs = mesylate) was identified as the most efficient precatalyst, facilitating the coupling of aryl chlorides with secondary and primary amines and indoles.

Automated summary

The study presented the synthesis and characterization of neutral and cationic N-methyl- and N-phenyl-2-aminobiphenyl methanesulfonate palladacycles stabilized with dialkylterphenyl phosphines. By selecting different phosphine ligands, different coordination modes and structures of complexes were obtained. The most efficient precatalyst, [Pd(N-methyl-2-aminobiphenyl)L4](OMs), was identified for facilitating the coupling of aryl chlorides with secondary and primary amines and indoles.