Heteroleptic copper(i) sensitizers with one versustwo hole-transporting units in functionalized 2,9-dimethyl-1,10-phenanthroline ancillary ligands

A series of homoleptic [Cu(L) sub(2)][PF sub(6)] complexes in which L is a 2,9-dimethyl-1,10-phenanthroline fused at the 5,6-positions with a 2'-functionalized imidazole (ligands 1-4), or substituted at the 4,7-positions with electron-donating 4-(diphenylamino)phenyl groups (ligand 5) is described; the imidazole 2'-functionality in 1 is 4-bromophenyl, in 2 is 4-(diphenylamino)phenyl, in 3 is 4-(bis(4-n-butoxy)phenylamino)phenyl, and in 4 is 4-(carbazol-9-yl)phenyl. The copper complexes were characterized by mass spectrometry, NMR and absorption spectroscopies and cyclic voltammetry; the single crystal structure of ligand 4 has been determined. Compared to the solution absorption spectra of [Cu(1) sub(2)][PF sub(6)], [Cu(2) sub(2)][PF sub(6)], [Cu(3) sub(2)][PF sub(6)] and [Cu(4) sub(2)][PF sub(6)], that of [Cu(5) sub(2)][PF sub(6)] shows increased absorbance at wavelengths >375 nm. An on-surface strategy was used to assemble heteroleptic [Cu(6)(L)] super(+) dyes on TiO sub(2) electrodes where 6 is ((6,6'-dimethyl-[2,2'-bipyridine]-4,4'-diyl)bi s(4,1-phenylene))bis(phosphonic acid); solid-state absorption spectra confirmed enhanced light-harvesting between 375 and 600 nm for [Cu(6)(5)] super(+) with respect to [Cu(6)(1)] super(+), [Cu(6)(2)] super(+), [Cu(6)(3)] super(+) and [Cu(6)(4)] super(+). Comparison of the performances of dye-sensitized solar cells (DSCs) containing [Cu(6)(2)] super(+), [Cu(6)(3)] super(+) and [Cu(6)(4)] super(+) with those with [Cu(6)(1)] super(+) indicate only a marginal influence of the diphenylamine or carbazole hole-transporting domains in 5,6-substituted phenanthroline dyes. The introduction of the 4-(diphenylamino)phenyl hole-transporting units in the 4- and 7-positions of the phen unit in 5 proves to be beneficial, with DSCs containing [Cu(6)(5)] super(+) performing better than those with the other four dyes; duplicate DSCs were tested for each dye to validate the results. While the values of the maximum external quantum efficiencies (EQE sub(max)) for [Cu(6)(1)] super(+) and [Cu(6)(4)] super(+) are greater than for [Cu(6)(5)] super(+), the extension of the EQE spectrum for [Cu(6)(5)] super(+) to longer wavelengths results in higher short-circuit current densities (J sub(SC)) compared to DSCs with [Cu(6)(1)] super(+), [Cu(6)(2)] super(+), [Cu(6)(3)] super(+) and [Cu(6)(4)] super(+).