A water-soluble cyclometalated iridium() complex for pH sensing based on aggregation-induced enhanced phosphorescence

The novel water-soluble monoanionic Ir( iii ) complex Na[Ir(ppy) 2 (SB-COO)] ( 2 ; Hppy = phenylpyridine; HSB-COOH = 4-carboxylanilinesalicylaldehyde Schiff base), which was obtained by the reaction of the novel Ir( iii ) complex [Ir(ppy) 2 (SB-COOH)] ( 1 ) with NaOEt, in its aqueous solution, showed hydrogen ion (H + )-responsive aggregation-induced enhanced phosphorescence (AIEP). Both these complexes exhibited very weak and relatively strong emissions in solution and solid states, respectively. The pH-responsiveness of 2 was evaluated from its emission spectra in aqueous solution in the pH range of 8.7-1.8. Above pH 6, 2 showed weak emission with a maximum at 508 nm. Upon decreasing the pH to 4.7, AIEP with a bathochromic shift to 618 nm was induced by the aggregation of 1 , whereby the intensity at 618 nm was increased approximately by 50-fold compared to that at pH 6.0. This enhancement is due to restrictions of the geometrical changes in the six-membered chelate ring of the ancillary ligand (Ir-N-C-C-C-O-) and of the intramolecular rotations in the excited state. The enhanced luminescence originates from spin-forbidden metal-to-ligand-ligand charge transfer ( 3 MLLCT). Below pH 2.8, the emission intensity decreased owing to the decrease in the population of the emissive complex 1 upon dissociation of the ancillary ligand from the Ir(ppy) 2 unit. The novel Na[Ir(ppy) 2 (SB-COO)] (Hppy = phenylpyridine; HSB-COOH = 4-carboxylanilinesalicylaldehyde Schiff base) in aqueous solution showed pH-responsive aggregation-induced enhanced phosphorescence (AIEP) by the formation of the protonated species [Ir(ppy) 2 (SB-COOH)].