Five new bisphosphoramide-based Ln(III) nitrate complexes [La-2(NO3)(6)L-3(I)](n) (1), [Ce-2(NO3)(6)L-3(I)](n) (2), [Sm-2(NO3)(6)L-3(II)](n), (3), Sm-2(NO3)(6)L-3(III) (4), and Er(NO3)(3)L-2(III) (5) [L-I = piperazine-1,4-diylbis(diphenyl phosphine oxide), L-II = N,N'-(ethane-1,2-diyl)bis(N-methyl-P,P-diphenylphosphinic amide, and L-II = N,N'-(ethane-1,2-diyl)bis(P,P-diphenylphosphinic amide)] have been synthesized and characterized by elemental analysis, IR spectroscopy, thermogravimetric analysis (TGA), and single crystal X-ray and powder diffractions. The results of the X-ray diffraction analysis revealed the new polymorph of L-III, and the structural diversity of the synthesized complexes in the solid state.
Complexes 1-3 display two-dimensional coordination polymers (2D-CP), containing layers with honeycomb (6, 3) topology. In these 2D-CPs, each Ln center (La, Ce, and Sm in 1, 2, and 3, respectively) could be considered as a triconnected node, linked by three bridging bisphosphoramide ligands as two-connecting linkers.
In contrast, 4 is a discrete binuclear complex, in which bidentate L ill ligand has two entirely different conformations: the syn-chelating and the anti bridging. Cationic complex 5 shows the monomeric structure, where bidentate L-III adopts the syn-chelating conformation.
A comprehensive luminescence investigation has been performed on free ligands and their corresponding complexes as well. The synthesized compounds display a variety of luminescence behavior, including the ligand-centered fluorescence in 1, 2, and 5, two distinct emission peaks in 1 and 2, characteristic Sm-centered f-f emission in 3 and 4, and excitation-dependent emission in L-III, 1, and 2.
Furthermore, the time dependent density functional theory (TD-DFT) study was carried out on the reported compounds to understand the nature of the emission peaks and the observed luminescence properties. The solid-state emission quantum yields of lanthanide complexes were also determined at different excitation wavelengths.