The designed synthesis of a sensitive phosphorescent chemosensor [Ir(ppy)2(L1)](PF6) (1) (Hppy = 2-phenylpyridine, L1 = 4′-methyl-2,2′-bipyridyl-4-carbaldehyde oxime) was carried out for selective detection of hypochlorite (ClO−). Complex 1 is weakly emissive in solution at ambient temperature due likely to rapid isomerization of C
N–OH as an effective non-radiative decay process. When 1 reacts with ClO−, however, the emission is remarkably enhanced, in which the oxime in L1 is converted to a carboxylic acid in L2 (4′-methyl-2,2′-bipyridine-4-carboxylic acid). The produced complex [Ir(ppy)2(L2)](PF6) (2) exhibits bright orange-yellow luminescence originating from [5d(Ir) → π*(bpy)] 3MLCT and [π(ppy) → π*(bpy)] 3LLCT triplet excited states as suggested from the DFT computational studies. The selective and competitive experiments reveal that complex 1 shows high sensing selectivity and sensitivity for ClO− over other reactive oxygen species (ROS) and metal ions.
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