LAUSR

Self-assembling the novel nitronyl nitroxide radical NIT-3Py-5-Ph (2-(5-phenyl-3-pyridyl)-4,4,5,5-tetramethylimidazoline-1-oxyl-3-oxide) with Ln(hfac)3·2H2O and Cu(hfac)2 (hfac = hexafluoroacetylacetonate) resulted in two heterometallic complexes with formula [LnCu(hfac)5(NIT-3Py-5-Ph)2] (Ln = Gd 1, Dy 2), in which two NIT-3Py-5-Ph radicals are coordinated with the LnIII ion via their nitroxide units in the cis-arrangement manner and the CuII ion is ligated by the pyridyl N donors of the radicals. Interestingly, when the phenyl group of NIT-3Py-5-Ph was replaced with a p-pyridyl group, a new family of 2D networks, namely, {[Ln(hfac)3][Cu(hfac)2]2(NIT-3Py-5-4Py)2}n (Ln = Gd 3, Tb 4, Dy 5; NIT-3Py-5-4Py = 2-(5-(4-pyridyl)-3-pyridyl)-4,4,5,5-tetramethylimidazoline-1-oxyl-3-oxide) was obtained. In the 2D sheet, each NIT-3Py-5-4Py ligand serves as a μ3-bridge to bind one LnIII center by the aminoxyl moiety and two CuII ions through two pyridine groups to form a 2D structure. The LnIII ion is coordinated by two NO units of two radicals in a trans configuration. DC magnetic measurements indicate that ferromagnetic LnIII-NO exchange occurs in 1-5. AC studies reveal that 2 displays slow relaxation of the magnetization while no such magnetic relaxation is found in complex 5. The observed different magnetic relaxation behaviors of two Dy analogues could be attributed to the different coordination modes of NO groups of the radicals, and the coordination geometry of the Dy center is from C2v in 2 to D2d in 5.