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Two types of the radical-3d-4f chains {[Cu(hfac)2][(NIT-4PyPh)]2[Ln(hfac)3]}n (Ln = Gd, 1; Tb, 2; Dy, 3) and {[Cu(hfac)2(NIT-4PyPh)]2Ln(hfac)3}n (Ln = Gd, 4; Tb, 5; Dy, 6; NIT-4PyPh = 2-[4-(4-pyridinylmethoxy)phenyl]-4,4,5,5-tetramethyl-imidazoline-1-oxyl-3-oxide; hfac = hexafluoroacetylacetonate) have been successfully achieved upon adjusting the experimental conditions. Compounds 1–3 display one-dimensional (1D) chain structure with NIT-4PyPh radical ligand bridging LnIII and CuII ions in “head-to-head” mode through pyridine-N atom and nitroxide unit of the radical. Complexes 4–6 possess an interesting 1D topological structure consisting of cyclic [Cu-Radical]2 dimers connected by Ln ions. Magnetic investigations indicate that ferromagnetic the copper(II)/lanthanide(III)-NO exchange occurs in two series of compounds. Furthermore, complexes 3 and 5 were found to exhibit frequency dependence of ac susceptibilities, evidencing slow magnetic relaxation.
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Sun et al. (2019) studied this question.
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