Six-coordinate tetracyanidonitridorhenium(V) and -technetium(V) with axial N-heteroaromatic ligands, (PPh4)2[MN(CN)4L] [M = Re, L = 4-(dimethylamino)pyridine (dmap), 3,5-lutidine (lut), 4-picoline (pic), 4-phenylpyridine (ppy), pyridine (py), 3-benzoylpyridine (3bzpy), 4,4′-bipyridine (bpy), pyrazine (pz), 4-cyanopyridine (cpy), or 4-benzoylpyridine (4bzpy); M = Tc, L = dmap, lut, pic, py, pz, or cpy] were synthesized and characterized. The crystal structures of 11 complexes were determined by single-crystal X-ray analysis. All of the complexes showed photoluminescence in the crystalline phase at room temperature. The emission maximum wavelengths (λem) of the rhenium complexes with dmap, lut, pic, ppy, or py were similar to one another with a quite high emission quantum yield (Φem): λem = 539-545 nm, Φem = 0.39-0.93, and emission lifetime (τem) = 10-45 μs at 296 K. The emission spectra at 77 K exhibited vibronic progressions, and the emissive excited state is characterized as 3[(dxy)1(dπ*)1] (dπ* = dxz, dyz). On the other hand, the emission maximum wavelength of the rhenium complex with 3bzpy, bpy, pz, cpy, or 4bzpy was significantly dependent on the nature of the axial ligand in the crystalline phase: λem = 564-669 nm, Φem ≤ 0.01-0.36, and τem = 0.03-13.3 μs at 296 K. The emission spectra at 77 K in the crystalline phase did not show vibronic progressions. The emissive excited state of the rhenium complex with bpy, pz, cpy, or 4bzpy is assignable to originate from the metal-to-N-heteroaromatic ligand charge-transfer (MLCT)-type emission with a spin-triplet type. The change in the excited-state characteristics of rhenium complexes by the N-heteroaromatic ligand is a result of stabilization of the π* orbital of the N-heteroaromatic ligand to a lower energy level than the dπ* orbitals. The emission spectral shapes of technetium complexes were almost independent of the nature of the N-heteroaromatic ligand with λem = 574-581 nm at room temperature. The different emission characteristics between the pz and cpy coordinate rhenium complexes and the technetium analogues would be due to stabilization of technetium-centered orbitals compared with the rhenium ones in energy.
ASJC Scopus subject areas
- Physical and Theoretical Chemistry
- Inorganic Chemistry