Dysprosium(III) chloride
Names | |
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IUPAC names
Dysprosium(III) chloride Dysprosium trichloride | |
Identifiers | |
10025-74-8 | |
3D model (Jmol) | Interactive image |
ChemSpider | 59592 |
ECHA InfoCard | 100.030.024 |
PubChem | 66207 |
UNII | Q2A03W637H |
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Properties | |
DyCl3 | |
Molar mass | 268.86 g/mol (anhydrous) |
Appearance | white solid |
Density | 3.67 g/cm3, solid |
Melting point | 647 °C (1,197 °F; 920 K) (anhydrous) |
Boiling point | 1,530 °C (2,790 °F; 1,800 K) |
Soluble | |
Structure | |
AlCl3 structure | |
Octahedral | |
Hazards | |
EU classification (DSD) |
not listed |
Flash point | Non-flammable |
Related compounds | |
Other anions |
Dysprosium(III) fluoride Dysprosium(III) bromide Dysprosium(III) iodide Dysprosium(III) oxide |
Other cations |
Terbium(III) chloride Dysprosium(II) chloride Holmium(III) chloride |
Related compounds |
Dysprosium(II) chloride |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
verify (what is ?) | |
Infobox references | |
Dysprosium(III) chloride (DyCl3), also known as dysprosium trichloride, is a compound of dysprosium and chlorine. It is a white to yellow solid which rapidly absorbs water on exposure to moist air to form a hexahydrate, DyCl3.6H2O. Simple rapid heating of the hydrate causes partial hydrolysis[1] to an oxychloride, DyOCl.
Preparation and reactions
DyCl3 is often prepared by the "ammonium chloride route," starting from either Dy2O3 or hydrated chloride or oxychloride.[2][3] or DyCl3·6H2O.[4] These methods produce (NH4)2[DyCl5]:
- 10 NH4Cl + Dy2O3 → 2 (NH4)2[DyCl5] + 6 NH3 + 3 H2O
- DyCl3·6H2O + 2 NH4Cl → (NH4)2[DyCl5] + 6 H2O
The pentachloride decomposes thermally according to the following equation:
- (NH4)2[DyCl5] → 2 NH4Cl + DyCl3
The thermolysis reaction proceeds via the intermediacy of (NH4)[Dy2Cl7].
Treating Dy2O3 with aqueous HCl produces hydrated chloride (DyCl3·6H2O). This salt cannot be rendered anhydrous by heating. Instead one obtains an oxychloride.
Dysprosium(III) chloride is a moderately strong Lewis acid, which ranks as "hard" according to the HSAB concept. Aqueous solutions of dysprosium chloride can be used to prepare other dysprosium(III) compounds, for example dysprosium(III) fluoride:
- DyCl3 + 3 NaF → DyF3 + 3 NaCl
Uses
Dysprosium(III) chloride can be used as a starting point for the preparation of other dysprosium salts. Dysprosium metal is produced when a molten mixture of DyCl3 in eutectic LiCl-KCl is electrolysed. The reduction occurs via Dy2+, at a tungsten cathode.[5]
Precautions
Dysprosium compounds are believed to be of low to moderate toxicity, although their toxicity has not been investigated in detail.
References
- ↑ F. T. Edelmann, P. Poremba, in: Synthetic Methods of Organometallic and Inorganic Chemistry, (W. A. Herrmann, ed.), Vol. 6, Georg Thieme Verlag, Stuttgart, 1997.
- ↑ Meyer, G. (1989). "The Ammonium Chloride Route to Anhydrous Rare Earth Chlorides-The Example of YCl3". Inorganic Syntheses. 25: 146–150. doi:10.1002/9780470132562.ch35. ISBN 978-0-470-13256-2.
- ↑ Edelmann, F. T.; Poremba, P. (1997). Herrmann, W. A. (ed.), ed. Synthetic Methods of Organometallic and Inorganic Chemistry. VI. Stuttgart: Georg Thieme Verlag. ISBN 3-13-103021-6.
- ↑ Taylor, M.D.; Carter, C.P. "Preparation of anhydrous lanthanide halides, especially iodides". Journal of Inorganic and Nuclear Chemistry. 24 (4): 387–391. doi:10.1016/0022-1902(62)80034-7.
- ↑ Y. Castrillejo, M. R. Bermejo, A. I. Barrado, R. Pardo, E. Barrado, A. M. Martinez, Electrochimica Acta, 50, 2047-2057 (2005).