From Handwiki
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| Names | |
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| IUPAC name
Iron(II) oxalate
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| Other names
Iron oxalate
Ferrous oxalate | |
| Identifiers | |
3D model (JSmol)
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PubChem CID
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| Properties | |
| FeC2O4 (anhydrous) FeC2O4 • 2H2O (dihydrate) | |
| Molar mass | 143.86 g/mol (anhydrous) 179.89 g/mol (dihydrate) |
| Appearance | yellow powder |
| Odor | odorless |
| Density | 2.28 g/cm3 |
| Melting point | dihydrate: 150–160 °C (302–320 °F; 423–433 K) (decomposes) |
| dihydrate: 0.097 g/100ml (25 °C)[1] | |
| Hazards | |
| GHS pictograms | [2]
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| GHS Signal word | Warning |
| H302, H312[2] | |
| P280[2] | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
| Infobox references | |
Ferrous oxalate (iron(II) oxalate) are inorganic compound with the formula FeC2O4(H2O)x where x is 0 or 2. These are orange compounds, poorly soluble in water. Thyy
Like other iron oxalates, ferrous oxalates feature octahedral Fe centers. The dihydrate FeC2O4(H2O)x is a coordination polymer, consisting of chains of oxalate-bridged ferrous centers, each with two aquo ligands.[3]
When heated to 120 °C, the dihydrate dehydrates, and the anhydrous ferrous oxalate decomposes near 190 °C.[4] The products of thermal decomposition is a mixture of iron oxides and pyrophoric iron metal, as well as released carbon dioxide, carbon monoxide, and water.[5]
Ferrous oxalates are precursors to iron phosphates, which are of value in batteries.[6]
Anhydrous iron(II) oxalate is unknown among minerals as of 2020. However, the dihydrate is known as humboldtine.[7][8] A related, though much more complex mineral is stepanovite,
Na[Mg(H2O)6] [Fe3+(C2O4)3]·3H2O - an example of trioxalatoferrate(III).[9][8]
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Categories: [Iron(II) compounds] [Oxalates] [Inorganic compounds]