Article ID Journal Published Year Pages File Type
1333219 Journal of Solid State Chemistry 2010 7 Pages PDF
Abstract

A new iron phosphate (NH4)4Fe3(OH)2F2[H3(PO4)4] has been synthesized hydrothermally at HF concentrations from 0.5 to 1.2 mL. Single-crystal X-ray diffraction analysis reveals its three-dimensional open-framework structure (monoclinic, space group P21/n (No. 14), a=6.2614(13) Å, b=9.844(2) Å, c=14.271(3) Å, β=92.11(1)°, V=879.0(3) Å3). This structure is built from isolated linear trimers of corner-sharing Fe(III) octahedra, which are linked by (PO4) groups to form ten-membered-ring channels along [1 0 0]. This isolated, linear trimer of corner-sharing Fe(III) octahedra, [(FeO4)3(OH)2F2], is new and adds to the diverse linkages of Fe polyhedra as secondary building units in iron phosphates. The trivalent iron at octahedral sites for the title compound has been confirmed by synchrotron Fe K-edge XANES spectra and magnetic measurements. Magnetic measurements also show that this compound exhibit a strong antiferromagnetic exchange below TN=17 K, consistent with superexchange interactions expected for the linear trimer of ferric octahedra with the Fe–F–Fe angle of 132.5°.

Graphical abstractThe three-dimensional open-framework structure of (NH4)4Fe3(OH)2F2[H3(PO4)4] is built from a novel isolated, linear (FeO4)3(OH)2F2 trimer of corner-sharing Fe(III) octahedra linked by PO4 tetrahedra.Figure optionsDownload full-size imageDownload as PowerPoint slide

Related Topics
Physical Sciences and Engineering Chemistry Inorganic Chemistry
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