Photochemical and Photophysical Reactions of fac-Rhenium(I) Tricarbonyl Complexes. Effect from Nucleating Spectator Ligands on Excited and Ground State Processes

J. GUERRERO; O. E. PIRO; E. WOLCAN; M. FÉLIZ; G. FERRAUDI; S. A. MOYA

ORGANOMETALLICS

American Chemical Society

Año: 2001 vol. 20 p. 2842 - 2853

0276-7333

Ground and excited state properties of the newly prepared complexes Re(CO)3(2,2¢-biquinoline) LS +, LS ) pyrazine or 4,4¢-bipyridine, and Re(CO)3(2,2¢-bipy)(2-pyrazinecarboxylate) were investigated by steady state and time-resolved spectroscopy. The X-ray structure of the latter compound showed that the spectator ligand 2-pyrazinecarboxylate is coordinated through the carboxylate group to Re(I). A component of the complexes’ luminescence was associated with long-lived Re to ligand, 2,2¢-biquinoline or 2,2¢-bipy, charge transfer, while a fast component of the emission was associated with intraligand excited states. Quenching of the luminescence by CuCl2 involved energy transfer via dynamic and static mechanisms. The complexes in their excited states were reduced by 2,2¢,2¢¢-nitrilotriethanol with the formation of Re(I) ligand-radical species. Similar products were generated by the pulse radiolytic reduction of the complexes. The photochemical properties of the 2,2¢-biquinoline complexes and Re(CO)3(1,10-phen)4-nitrobenzoate are compared, and the mechanisms of their photochemical reactions are discussed.