Abstract
A new organically templated iron(II) phosphatooxalate, (N2C 4H12)[Fe4(C2O4) 3(HPO4)2(H2O)], I has been synthesized under hydrothermal conditions, in which oxalate groups act as bidentate ligands to Fe and hold the structure together by strong interlayer Pa-Oa-H-oxalate hydrogen bonds. A new organically templated iron(II) phosphatooxalate, (N2C4H12)[Fe 4(C2O4)3(HPO4) 2(H2O)2] I, has been synthesized under hydrothermal conditions and characterized by single-crystal X-ray diffraction. The structure possesses infinite chains made from Fe2O10 dimers and PO4 tetrahedra bridged by bidentate oxalate units and strong interlayer Pa-Oa-H-oxalate hydrogen bonds. The diprotonated piperazinium cations are located in the intersecting tunnels parallel to the [1 0 0] and [0 1 0] directions.
| Original language | English |
|---|---|
| Pages (from-to) | 2357-2362 |
| Number of pages | 6 |
| Journal | Polyhedron |
| Volume | 23 |
| Issue number | 15 |
| DOIs | |
| State | Published - 30 Sep 2004 |
| Externally published | Yes |
Keywords
- Crystal structure
- Hydrothermal synthesis
- Iron phosphatooxalate
- Oxalate acid
- Piperazine
- Template
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