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Praseodymium(III) chloride
| praseodymium(III) chloride heptahydrate | |
| IUPAC name praseodymium(III) chloride | |
| General | |
|---|---|
| Molecular formula | PrCl3 |
| Molecular weight | 247.24 amu (anhydrous)
373.77 amu (heptahydrate) |
| Appearance | blue-green solid (anhydrous)
light green solid (heptahydrate) |
| CAS number | [10361-79-2] (anhydrous)
[10025-90-8] (heptahydrate) |
| MSDS | Praseodymium(III) chloride MSDS |
| Other names | |
| |
| Bulk properties | |
| Density | 4.02 g/cm3 (anhydrous) |
| Solubility | water: 104.0 g/100 cm3 (13 °C)
ethanol: soluble pyridine: soluble chloroform: insoluble ether: insoluble |
| Melting point | 786 °C (1059 K) |
| Boiling point | 1710 °C (1980 K) |
| Hazards: | Irritant |
| Structure | |
| Coordination geometry | nine-coordinate (trigonal prismatic) |
| Crystal structure | UCl3 |
| Hydrates | heptahydrate |
| Related compounds | |
| praseodymium fluoride
praseodymium bromide praseodymium iodide | cerium(III) chloride |
| Contents |
Overview
Praseodymium(III) chloride (PrCl3), also known as praseodymium trichloride, is a compound of praseodymium and chlorine. It is a blue-green solid which rapidly absorbs water on exposure to moist air to form a light green heptahydrate.
Chemical properties
Praseodymium(III) chloride can be prepared as a green aqueous solution by reaction of either praseodymium metal or praseodymium(III) carbonate and hydrochloric acid. The anhydrous halide may alternatively be prepared from praseodymium metal and hydrogen chloride[6].
2 Pr(s) + 6 HCl(aq) → 2 PrCl3(aq) + 3 H2(g)
Pr2(CO3)3 (s) + 6 HCl(aq) → 2 PrCl3(aq) + 3 CO2(g) + 3 H2O(l)
Praseodymium(III) chloride is a moderately strong Lewis acid, which ranks as "hard" according to the Hard-Soft Acid-Base theory . Rapid heating of the hydrate may cause small amounts of hydrolysis [1].
Preparation
Aqueous solutions of praseodymium(III) chloride can be used to prepare insoluble praseodymium(III) compounds, for example praseodymium(III) phosphate or praseodymium(III) fluoride:
PrCl3(aq) + K3PO4 (aq) → PrPO4(s) + 3 KCl(aq)
PrCl3(aq)aq + 3 NaF(aq) → PrF3(s) + 3 NaCl(aq)
Anhydrous PrCl3 can be made by dehydration of the hydrate either by slowly heating to 400 °C with 4-6 equivalents of ammonium chloride under high vacuum[1],[4], or by heating with an excess of thionyl chloride for four hours[1],[5]. The anhydrous halide may alternatively be prepared from praseodymium metal and hydrogen chloride [6]. It is usually purified by high temperature sublimation under high vacuum. [1]
Uses
There are no major uses for praseodymium(III) chloride, though it can be used as a starting point for the preparation of other praseodymium salts.
Precautions
Praseodymium compounds are of low to moderate [[toxicity], although their toxicity has not been investigated in detail. Wear gloves and goggles.
Suppliers/Manufacturers
GFS: http://www.gfschemicals.com/productcatalog/Rare_Earth_Compounds_PT.asp
Aldrich: http://www.sigmaaldrich.com
Strem: http://www.strem.com/code/index.ghc
Alfa: http://www.alfa.com/alf/index.htm
In the US, several of these suppliers also distribute through VWR: http://www.vwr.com/index.htm or Fisher: https://www1.fishersci.com/index.jsp
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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.
- CRC Handbook of Chemistry and Physics (58th edition), CRC Press, West Palm Beach, Florida, 1977.
- N. N. Greenwood, A. Earnshaw, Chemistry of the Elements, Pergamon Press, 1984.
- M. D. Taylor, P. C. Carter, J. Inorg. Nucl. Chem. 24, 387 (1962); J. Kutscher, A. Schneider, Inorg. Nucl. Chem. Lett. 7, 815 (1971).
- J. H. Freeman, M. L. Smith, J. Inorg. Nucl. Chem. 7, 224 (1958).
- L. F. Druding, J. D. Corbett, J. Am. Chem. Soc. 83, 2462 (1961); J. D. Corbett, Rev. Chim. Minerale 10, 239 (1973).
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