Abstract
Two new metal borates, K[B7O9(OH)5]·Hen (1, en = enthylenediamine) and Na2Cs4Ba2[B12O18(OH)6]·4(OH) (2) have been synthesized under solvothermal conditions. Their structures were determined by the single crystal X-ray diffraction and were further characterized by elemental analysis, IR spectroscopy, thermogravimetric analysis and powder X-ray diffraction, respectively. 1 crystallizes in the triclinic system, P-1 space group, a = 7.7152(6), b = 8.4057(6), c = 12.1319(10) Å, α = 92.505(6), β = 98.944(7), γ = 103.825(6)°, Z = 2. 2 crystallizes in the orthorhombic system, Pmn21 space group, a = 12.6972(6) Å, b = 13.7037(6) Å, c = 9.4968(5) Å, Z = 2. Compound 1 consists of isolated [B7O9(OH)5]2− clusters which are held together through H-bonding interactions and K atoms to form a 3-D supramolecular framework. For 2, bowl-like isolated [B12O18(OH)6]6− clusters were linked together to form a 3-D framework by different metal ions and H-bond system.
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Zhang, TJ., Pan, R., He, H. et al. Solvothermal Synthesis and Structure of Two New Borates Containing [B7O9(OH)5]2− and [B12O18(OH)6]6− Clusters. J Clust Sci 27, 625–633 (2016). https://doi.org/10.1007/s10876-015-0962-y
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DOI: https://doi.org/10.1007/s10876-015-0962-y