Two new iron(III) oxalatophosphates, Cs2Fe(C20 4)0.5(HPO4)2 (1) and CsFe(C 2O4)0.5(H2PO4)(HPO 4) (2), have been synthesized by using a low melting point eutectic mixture of choline chloride and malonic acid as a solvent and characterized by single-crystal X-ray diffraction and magnetic susceptibility. Crystal data are as follows: compound 1, monoclinic, P21/c(No. 14), a = 8.5085(4) A, b = 12.7251(6) Å, c = 9.8961(4) Å, β = 107.117(1)°, V = 1024.01(8) Å3, Z = 4, and R1 = 0.0264; compound 2, monoclinic, P21/n (No. 14), a = 8.0038(3) Å, b = 10.2923(3) Å, c = 11.4755-(4) Å, β = 100.507(1)°, V = 929.47(5) Å3, Z = 4, and R1 = 0.0311. The structure of 1 comprises FeO6 octahedra connected by HPO42- tetrahedra and bisbidentate oxalate anions to form a 3D framework containing intersecting 12-ring channels, with the charge-compensating Cs+ cations being located at the intersections of these channels. The structure of 2 consists of 2D layers of octahedral FeO6, tetrahedral H 2PO4- and HPO42- moieties, and bisbidentate oxalate ligands with the Cs+ cations between the layers. They are the first examples for the use of ionic liquid as a solvent in the synthesis of metal oxalatophosphates.
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Sheu, C. (Contributor), Lii, K. (Contributor) & Lee, S. (Contributor), The Cambridge Structural Database, 1 Jan 2006
Sheu, C. (Contributor), Lee, S. (Contributor) & Lii, K. (Contributor), The Cambridge Structural Database, 1 Jan 2006