Abstract

Two new iron(II) coordination polymers with the formula [Fe(TPOM)(SCN)2]·2(HN(CH3)2)·4(H2O) (1, TPOM = tetrakis(4-pyridyloxymethylene)methane) and [Fe(TPOM2)(SCN)2]·2(CH3OH) (2, TPOM2 = tetrakis(3-pyridyloxymethylene)methane), have been synthesized and characterized by elemental analysis, IR spectroscopy, TGA, magnetic measurements and X-ray single-crystal diffraction. Compound 1 crystallizes in the orthorhombic space group Cccm, and exhibits a 3D porous pts framework in which the FeII(NCS)2 units are linked by the tetra-topic TPOM ligands. In contrast, compound 2 crystallizes in the monoclinic space group C2/c, whose crystal structure consists of a 2D sheet formed by the connection of FeII(NCS)2 units and tetra-topic TPOM2 ligands. Interestingly, every 2D sheet interleavingly stacks over each other to totally construct a [4] tiling structure with a plane net signature of [122]4[4·4·4·4]. Temperature-dependent SQUID under variable external pressure and X-ray diffraction measurements indicate that the iron(II) ions in 1 and 2 remain in the high spin state over the temperature range of 2–300 K.

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