ABSTRACT
A new iminophosphonamine Ph2P(HNPbt)(NPbt) (1, HL) bearing chromophore 2-(phen-2'-yl)-1,3-benzothiazole (Pbt) substituents was synthesized and introduced into lanthanide complexes. It was found that salt metathesis reactions between KL (2) generated in situ and LnCl3 lead to the formation of tris-iminophosphonamide complexes [LnL2]L (Ln = Y (3), Sm (4), Gd (5), Dy (6)), regardless of the 2/LnCl3 ratio. Compounds 3-6 consist of a cationic fragment [LnL2]+, where the lanthanide atom is surrounded by two rigidly κ4-coordinated ligands, and an L- anion residing in the outer coordination sphere. Iminophosphonamine 1 shows a rare excitation wavelength-dependent two-band luminescence in the solid state. For compounds containing the deprotonated form, namely potassium salt KL and complexes of Gd and Dy, a single-band luminescence with the color changing from turquoise to orange was observed. The Sm complex reveals a set of a few narrow well-resolved bands corresponding to the f-f transitions against the background of the outer-sphere ligand's emission.
