4.7 Article

Solvothermal syntheses, crystal structures and luminescence properties of three new lanthanide sulfate fluorides

Journal

DALTON TRANSACTIONS
Volume 39, Issue 15, Pages 3681-3686

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/b926131a

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Funding

  1. National Natural Science Foundation of China [20771050, 20771059, 20971068]

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Three novel lanthanide sulfate fluorides of formulae [C4H16N3](6)[Sm4F2(SO4)(14)] 1 and LnFSO(4)center dot H2O (Ln = Tb 2; Nd 3) have been synthesized solvothermally and structurally characterized by single-crystal X-ray diffraction, IR, TGA, SEM, and ICP. Single crystal X-ray diffraction reveals that compound 1 crystallizes in the triclinic crystal system, with space group P-1 and cell dimensions: a = 11.1988(9), b = 11.4073(9), c = 16.2666(13) angstrom, alpha = 89.9010(10)degrees, beta = 82.4060(10)degrees, gamma = 67.7570(10)degrees, V = 1903.9(3) angstrom(3), Z = 1. Both compounds 2 and 3 crystallize in the monoclinic crystal system, with the space group P2(1)/n and cell dimensions: a = 5.0014(7), b = 7.3769(11), c = 11.6508(17) angstrom, beta = 96.692(2)degrees, V = 426.93(11) angstrom(3), Z = 4 for 3; a = 4.9948(5), b = 7.3684(7), c = 11.6366(12) angstrom, beta = 96.6720(10)degrees, V = 425.37(7) angstrom(3), Z = 4 for 3. The structure of 1 consists of a novel isolated large Z-type heteropolyanion [Sm4F2(SO4)(14)](18-) and full protonated organic amine cations. The chains are held together by hydrogen bond interactions involving the hydrogen of the amine and the framework oxygen. The compounds 2 and 3 are isostructural and their structures feature a three-dimensional network constructed from the left-handed and the right-handed helical channels which are connected by SO42- groups using 6-membered rings and 4-membered rings.

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