4,5-diazafluorene (daf) and 9,9'-dimethyl-4,5-diazafluorene (Me₂daf) are structurally similar to the important ligand 2,2'-bipyridine (bpy), but significantly less is known about the redox and spectroscopic properties of metal complexes containing Me₂daf as a ligand than those containing bpy. New complexes Mn(CO)₃Br(daf) (2), Mn(CO)₃Br(Me₂daf) (3), and [Ru(Me₂daf)₃](PF₆)₂ (5) have been prepared and fully characterized to understand the influence of the Me₂daf framework on their chemical and electrochemical properties. Structural data for 2, 3, and 5 from single-crystal X-ray diffraction analysis reveal a distinctive widening of the daf and Me₂daf chelate angles in comparison to the analogous Mn(CO)₃(bpy)Br (1) and [Ru(bpy)₃]²⁺ (4) complexes. Electronic absorption data for these complexes confirm the electronic similarity of daf, Me₂daf, and bpy, as spectra are dominated in each case by metal-to-ligand charge transfer bands in the visible region. However, the electrochemical properties of 2, 3, and 5 reveal that the redox-active Me₂daf framework in 3 and 5 undergoes reduction at a slightly more negative potential than that of bpy in 1 and 4. Taken together, the results indicate that Me₂daf could be useful for preparation of a variety of new redox-active compounds, as it retains the useful redox-active nature of bpy but lacks the acidic, benzylic C-H bonds that can induce secondary reactivity in complexes bearing daf.

Micah L. Anderson

Publications