NITROSYL NITRO REDOX COUPLES WITH METAL PHTHALOCYANINES - SYNTHESIS AND CHARACTERIZATION OF NITRO-DERIVATIVES OF COBALT AND IRON PHTHALOCYANINE, DIOXYGEN ACTIVATION, OXYGEN-ATOM TRANSFER AND STOICHIOMETRIC AND CATALYTIC-OXIDATION OF TERMINAL OLEFINS

The complexes [Co(pc)(NO2)(py)].dce, [Co(pc)(NO2)(py)].thf, and [Fe(pc)(NO2)(py)] (pc = phthalocyaninate, py = pyridine, dce = 1,2-dichloroethane and thf = tetrahydrofuran) have been isolated as stable crystalline materials. Their molecular and electronic structures have been investigated by IR and UV/VIS spectra, X-ray powder patterns, thermogravimetric and magnetic susceptibility measurements and Mossbauer spectra. The complexes should be regarded as six-co-ordinate low-spin cobalt(III) and iron(III) species. Reference is also made to their corresponding five-co-ordinate nitrosyl derivatives, [Co(pc)(NO)] and [Fe(pc)(NO)]. The Co(pc)- and Fe(pc)-NO/NO2 systems have been studied with regard to their dioxygen activation and oxygen-atom-transfer reactions, in the oxidation of terminal olefins to the corresponding methyl ketones. Whereas oxidation with the Co(pc)-NO/NO2 redox couple is nearly stoichiometric, catalytic and selective oxidation occurs with the parallel Fe(pc) system.