Titanium(III) fluoride
(Redirected from Titanium trifluoride)
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| Names | |
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| IUPAC name
Titanium(III) fluoride | |
Other names
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| Identifiers | |
3D model (JSmol) |
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| ChemSpider | |
| ECHA InfoCard | 100.033.379 |
| EC Number |
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PubChem CID |
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CompTox Dashboard (EPA) |
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| Properties | |
| TiF3 | |
| Molar mass | 104.862 g·mol−1 |
| Appearance | violet to purple-red powder |
| Density | 2.98 g/cm3 |
| Melting point | 1,200 °C (2,190 °F; 1,470 K) |
| Boiling point | 1,400 °C (2,550 °F; 1,670 K) |
| soluble | |
| 1.3×10−9 cm3/mol | |
| Structure | |
| Rhombohedral, hR24 | |
| R-3c, No. 167 | |
| Hazards | |
| Occupational safety and health (OHS/OSH): | |
Main hazards |
Corrosive |
| GHS labelling:[1] | |
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| Danger | |
| H314 | |
| P260, P280, P303+P361+P353, P304+P340+P310, P305+P351+P338, P363 | |
| NFPA 704 (fire diamond) | |
| Related compounds | |
Other anions |
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Related compounds |
Titanium(IV) fluoride |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Titanium(III) fluoride is the inorganic compound with the formula TiF3. A violet, paramagnetic solid, it is one of two titanium fluorides, the other being titanium tetrafluoride.[3] It adopts a defect perovskite-like structure such that each Ti center has octahedral coordination geometry, and each fluoride ligand is doubly bridging.[4]
Titanium(III) fluoride can be prepared by dissolution of titanium metal in hydrofluoric acid. It oxidizes to Titanium dioxide (TiO2) above 100 °C (212 °F) in air.[3]
References
[edit]- ↑ Sigma-Aldrich Co., Titanium (III) fluoride.
- ↑ "SDS - Titanium (III) fluoride". thermofisher.com. ThermoFisher Scientific. 26 March 2024. p. 3. Retrieved 25 October 2025.
- 1 2 Meshri, Dayal T. (2000). "Fluorine Compounds, Inorganic, Titanium". Kirk-Othmer Encyclopedia of Chemical Technology. doi:10.1002/0471238961.2009200113051908.a01. ISBN 978-0-471-48494-3.
- ↑ H. Sowa; H. Ahsbahs (1998). "Pressure-Induced Octahedron Strain in VF3-Type Compounds". Acta Crystallogr. B54 (5): 578–584. Bibcode:1998AcCrB..54..578S. doi:10.1107/S0108768198001207.
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