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https://www.selleckchem.com/products/ms-275.html A series of 3D homologous metal-organic frameworks, [M(H0.5L)2] [M = Dy (1), Ho (2), Yb (3), Sm (4), Gd (5), and Y (6); H2L = 5-(1H-imidazol-1-yl)isophthalic acid], were isolated. In these complexes, the metal centers behave as hexacoordinated environments with distorted octahedral geometries, which is unusual in the lanthanide series, linking to each other and producing a fascinating 3D architecture. Magnetically, 1 features a field-driven dual-magnetic relaxation, which is rarely observed in high-dimensional coordination polymers. Analysis on the dilution sample (1@Y) and ab initio calculation unveil that the thermally assisted slow relaxation is mostly caused by the single-ion magnetism of DyIII itself.The phase relations in the subsolidus region of the Tl2MoO4-Bi2(MoO4)3-Hf(MoO4)2 system were studied with the "intersecting cuts" method. The formation of the novel ternary molybdate Tl5BiHf(MoO4)6 is found in this ternary system. The compound has a phase transition at Tpt = 731 K (ΔH = -3.15 J/g) and melts at Tm = 871 K (ΔH = -41.71 J/g), as determined by a thermal analysis. Tl5BiHf(MoO4)6 single crystals were obtained by the spontaneous nucleation method. The crystal structure of Tl5BiHf(MoO4)6 was revealed by structure analysis methods. This molybdate crystallizes in the trigonal space group R3̅c with the unit cell parameters a = 10.6801(4) Å, c = 38.5518(14) Å, V = 3808.3(2) Å3, and Z = 6. The vibrational characteristics of Tl5BiHf(MoO4)6 were determined by Raman spectroscopy. The Tl5BiHf(MoO4)6 conductivity was measured at frequencies of 0.1, 1.0, and 10 kHz in the temperature range of 293-773 K; in this temperature range, the conductivity level was 10-12-10-7 S/cm.The oxyhalide-based solid electrolyte Li2OHCl usually forms the thermodynamically stable orthorhombic phase at room temperature and shows poor lithium ionic conductivity. Above 35 °C, a structural phase transition into the cubic phase occurs and ionic

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