Shine bright or live long: substituent effects in [Cu((NN)-N-boolean AND)((PP)-P-boolean AND)]+-based light-emitting electrochemical cells where (NN)-N-boolean AND is a 6-substituted 2,2'-bipyridine

摘要

We report [Cu(P boolean AND P)(N boolean AND N)][PF6] complexes with P boolean AND P = bis(2-(diphenylphosphino) phenyl) ether (POP) or 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene (xantphos) and N boolean AND N = 6-methyl-2,2'-bipyridine (Mebpy), 6-ethyl-2,2'-bipyridine (Etbpy), 6,6'-dimethyl-2,2'-bipyridine (Me(2)bpy) or 6-phenyl-2,2'-bipyridine (Phbpy). The crystal structures of [Cu(POP)(Phbpy)][PF6]center dot Et2O, [Cu(POP)(Etbpy)][PF6]center dot Et2O, [Cu(xantphos)(Me(2)bpy)][PF6], [Cu(xantphos)(Mebpy)][PF6]center dot CH2Cl2 center dot 0.4Et(2)O, [Cu(xantphos)(Etbpy)][PF6]center dot CH2Cl2 center dot 1.5H(2)O and [Cu(xantphos)(Phbpy)][PF6] are described; each copper(I) centre is distorted tetrahedral. In the crystallographically determined structures, the N boolean AND N domain in [Cu(xantphos)(Phbpy)](+) and [Cu(POP)(Phbpy)](+) is rotated similar to 180 degrees with respect to its orientation in [Cu(xantphos)(Mebpy)](+), [Cu(POP)(Etbpy)](+) and [Cu(xantphos)(Etbpy)](+); in each complex containing xantphos, the xanthene 'bowl' retains the same conformation in the solid-state structures. The two conformers resulting from the 180 degrees rotation of the N boolean AND N ligand were optimized at the B3LYP-D3/(6-31G**+ LANL2DZ) level and are close in energy for each complex. Variable temperature NMR spectroscopy evidences the presence of two conformers of [Cu(xantphos)(Phbpy)](+) in solution which are related by inversion of the xanthene unit. The complexes exhibit MLCT absorption bands in the range 378 to 388 nm, and excitation into each MLCT band leads to yellow emissions. Photoluminescence quantum yields (PLQYs) increase from solution to thin-film and powder; the highest PLQYs are observed for powdered [Cu(xantphos)(Mebpy)][PF6] (34%), [Cu(xantphos)(Etbpy)][PF6] (37%) and [Cu(xantphos)(Me2bpy)][PF6] (37%) with lifetimes of 9.6-11 mu s. Density functional theory calculations predict that the emitting triplet (T1) involves an electron transfer from the Cu-P boolean AND P environment to the N boolean AND N ligand and therefore shows a (MLCT)-M-3 character. T1 is calculated to be similar to 0.20 eV lower in energy than the first singlet excited state (S1). The [Cu(P boolean AND P)(N boolean AND N)][PF6] ionic transitionmetal (iTMC) complexes were tested in light-emitting electrochemical cells (LECs). Turn-on times are fast, and the LEC with [Cu(xantphos)(Me2bpy)][PF6] achieves a maximum efficacy of 3.0 cd A(-1) (luminance = 145 cd m(-2)) with a lifetime of 1 h; on going to the [Cu(xantphos)(Mebpy)][PF6]-based LEC, the lifetime exceeds 15 h but at the expense of the efficacy (1.9 cd A(-1)). The lifetimes of LECs containing [Cu(xantphos)(Etbpy)][PF6] and [Cu(POP)(Etbpy)][PF6] exceed 40 and 80 h respectively.