Selective ortho C-h activation of haloarenes by an Ir(I) system.

The cationic PNP-Ir(I)(cyclooctene) complex 1 (PNP = 2,6-bis-(di-tert-butyl phosphino methyl)pyridine) reacts with benzene at 25 degrees C to quantitatively yield the crystallographically characterized, square pyramidal, iridium phenyl hydride complex cis-(PNP)Ir(Ph)(H), 2, in which the hydride is trans to the vacant coordination site. The cationic complex 2 is stable to heating at 100 degrees C, in sharp contrast to the previously reported unstable neutral, isoelectronic (PCP)Ir(H)(Ph) (PCP = eta(3)-2,6-((t)()Bu(2)PCH(2))(2)C(6)H(3)). Heating of 2 at 50 degrees C with other arenes results in arene exchange. Complex 1 activates C-H bonds of chloro- and bromobenzene with no C-halide oxidative addition being observed. Selective ortho C-H activation takes place, the process being directed by halogen coordination and being thermodynamically and kinetically favorable. The meta- and para-C-H activation products are formed at a slower rate than the ortho isomer and are converted to it. NMR data and an X-ray crystallographic study of the ortho-activated chlorobenzene complex, which was obtained as the only product upon heating of 1 with chlorobenzene at 60 degrees C, show that the chloro substituent is coordinated to the metal center.