Two 3D metal–organic frameworks with different topologies, thermal stabilities and magnetic properties
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Abstract
Two novel 3D metal–organic frameworks, [ML]n (M = Co, 1; Mn, 2) were successfully prepared in solvothermal conditions using 3,3′-dimethoxy-4,4′-biphenyldicarboxylic acid (H2L) as the ligand. X-Ray crystallography analysis reveals that MOF 1 crystallizes in the monoclinic system, space group P21/c in contrast to MOF 2 in the tetragonal system, space group I. MOF 1 contains an elongated [CoO6] octahedron with two bound methoxy groups in the trans position, whereas MOF 2 has a compressed [MnO6] octahedron with two coordinated methoxy groups in the cis arrangement. The ligand L shows a novel bis(tridentate) bridging coordination mode. MOF 1 exhibits a 3D framework with CdSO4 (cds) topology consisting of two different nodes and good thermal stability (313 °C). MOF 2 is a doubly interpenetrated 3D α-Po framework with a higher thermal stability (368 °C). The study of magnetic properties in the temperature range of 1.8–300 K shows the occurrence of weak ferromagnetic interactions (J = 0.15 K) between the high-spin Co(II) ions in 1, but a weak antiferromagnetic coupling (J = −0.15 cm−1) between Mn(II) ions in 2 due to the syn-anti carboxylate bridge.
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