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Three 2D new coordination polymers Co2(L1)2(1,10-Phenanthroline)2(DMF)0.5(H2O) (1), (H2L1 = Pyridine-3,5-dicarboxylic acid) Co(L1)(2,2-bipyridine) (2), and Co(L2)(2,2-bipyridine) (DMF) (3) (H2L2 = Pyridine-3,4-dicarboxylic acid) were synthesized through a solvothermal reaction of cobalt nitrate and pyridine carboxylic acid ligand with the auxiliary ligand (1,10-Phenanthroline or 2,2-bipyridine). They were characterized by X-ray diffraction and elemental analysis, infrared spectroscopy, thermogravimetry analysis, and magnetism. Compounds 1&ndash, 3 featured 2D hexagonal (6,3) networks which linked into 3D supramolecular architectures through &pi, &ndash, &pi, interaction. In addition, compounds 1 and 2 showed the antiferromagnetic exchange interactions, and the magnetic property of compound 3 exhibited ferromagnetic exchange interactions.

An Mg-doped isotope lithium niobate (Mg:7LiNbO3) crystal was successfully grown from 7LiOH, Nb2O5, and MgO using the Crozchralski method. The weight of the as-grown crystal with good quality was about 40 g. The crystal structure was determined as an R3c space group using the X-ray powder diffraction (XRPD) method, and the crystal composition (Li%) determined using the Raman mode linewidth method was 49.29%. The average transmittance of the crystal in the range of 500&ndash, 2500 nm was approximately 72%. Various thermal properties, including the specific heat (Cp), the thermal expansion coefficient (&alpha, ), the thermal diffusion coefficient (&lambda, ), and the thermal conductivity (&kappa, ), were carefully determined and calculated, and the value divergences among Mg:7LiNbO3, the undoped isotope lithium niobate (7LiNbO3), and natural lithium niobate (LiNbO3) crystals were mainly related to the differences in microstructure caused by the crystal composition.