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The new radical ligand 5,8-dimethyl-1,4-dioxonaphtho[2,3- d ][1,2,3]dithiazolyl ( 1 ) is reported. Two crystal polymorphs, 1α and 1β, differing in their pancake-bonded dimerization motif and S···O contact network, are identified. The self-assembly of Mn(II) metal ions with 1 leads to the formation of [Mn(hfac) 2 ] 3 (1) 2 that exhibits a Mn(II)–radical–Mn(II)–radical–Mn(II) linear arrangement of three Mn(hfac) 2 units bridged by two radical ligands (hfac = 1,1,1,5,5,5-hexafluoroacetylacetonato-). Characterization by single-crystal X-ray diffraction of this Mn(II) complex packing structure reveals close noncovalent S···O contacts between the [Mn(hfac) 2 ] 3 (1) 2 units in one dimension along the b–c direction. The magnetic properties of the coordination complex are characterized by dc and ac susceptibility measurements on a microcrystalline solid. The magnetic data down to 4.8 K indicate the presence of effective ferromagnetic interactions ( J / k B = +0.16 K) between the molecular S T = 13/2 units along the supramolecular chain involving noncovalent S···O contacts. Below 2.9 K, a non-zero out-of-phase component appears in the ac susceptibility, indicating the presence of a three-dimensional magnetic phase transition.
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Mayo et al. (2021) studied this question.
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