Pt(II), Pd(II), and Ni(II) Complexes with Tridentate Cyclometalating Five- and Six-Ring Chelating N∧C*N, C∧N*N, and N*C*N Quinolinyl Ligands

Nine cyclometalated Ni(II), Pd(II), and Pt(II) complexes of the type [M(NCN)Cl] and [M(CNN)X] (X = Cl for Pt and Pd, or Br for Ni) containing 8-quinolinyl (Q), 2-pyridyl (Py), and phenyl (Ph) moieties are presented. The introduction of Q leads to six-ring chelates (N*C or N*N) compared with five-ring chelates ((CN)-N-boolean AND or (NN)-N-boolean AND) for 2-pyridyl-containing systems in the PyPhQ(-) ((NC)-C-boolean AND*N), QPhQ(-) (N*C*N), and PhPyQ(-) ((CN)-N-boolean AND*N) ligands. Single-crystal X-ray diffractometry showed the six-ring chelate units with angles around 90 degrees compared with 80 degrees for the five-ring chelates. Marked tilts of the planar Q systems toward the central Py or Ph core (up to 37 degrees) were observed. Cyclic voltammetry showed first reduction potentials varying from -1.8 to -2.2 V vs ferrocene/ferrocenium and oxidations at around 0.45 V for Pt, 0.75 V for Pd, and 0 V for Ni complexes. DFT-calculated energies and compositions of the frontier molecular orbitals allowed assigning reductions to ligand-centered processes and oxidations to processes with mixed X(p)/M(d)/Ph(pi) contributions. Long-wavelength UV-vis absorption maxima ranging from 400 to 430 nm were assigned to mixed ligand-centered(pi-pi*)/metal(d)-to-ligand(pi*) transitions. The new complex [Pt(PyPhQ)Cl] showed very long-wavelength photoluminescence (>600 nm), similar to that of the previously reported [Pt(QPhQ)Cl] derivative.