Sensitised near-IR lanthanide luminescence exploiting anthraquinone-derived chromophores: syntheses and spectroscopic properties

The syntheses of two anthraquinone-derived tetraaza macrocyclic ligands (L1 via 1-amino-9,10-anthraquinone and L2 via 1-amino-4-hydroxy-9,10-anthraquinone) together with their corresponding Ln(III) complexes, Ln-L1/2 (Ln = Nd-III, Gd-III, Er-III, Yb-III), are described. Both Ln-L1 (lambda(max) approximate to 380 nm) and Ln-L2 (lambda(max) approximate to 450 nm) complexes absorb in the visible region with good extinction coefficients (epsilon(vis) > 2 x 10(3) M-1 cm(-1)). Phosphorescence measurements on Gd-L1/2 at 77 K allowed the ligand-centred triplet states to be estimated at ca. 22000 cm(-1) and 19800 cm(-1) for Gd-L1 and Gd-L2 respectively. Steady state and time-resolved measurements showed that both chromophores sensitised Nd-III, Er-III and Yb-III ions, resulting in observable near-IR emission. Preliminary studies on the pH-dependent behaviour of the L2 derivatives demonstrated that deprotonation of the 4-hydroxyl group at pH 12 resulted in a significant bathochromic shift in the absorption pro. le, thus allowing sensitised near-IR emission utilising lambda(ex) = 575 nm.