Samarium(III) chloride

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Samarium(III) chloride
Samarium(III) chloride hexahydrate.jpg
UCl3 without caption.png
Names
IUPAC name
samarium(III) chloride
Other names
samarium trichloride
trichlorosamarium
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.030.712 OOjs UI icon edit-ltr-progressive.svg
EC Number
  • 233-797-0
PubChem CID
UNII
  • InChI=1S/3ClH.Sm/h3*1H;/q;;;+3/p-3 Yes check.svgY
    Key: BHXBZLPMVFUQBQ-UHFFFAOYSA-K Yes check.svgY
  • InChI=1/3ClH.Sm/h3*1H;/q;;;+3/p-3
    Key: BHXBZLPMVFUQBQ-DFZHHIFOAZ
  • Cl[Sm](Cl)Cl
Properties
SmCl3
Molar mass 256.76 g/mol (anhydrous)
364.80 g/mol (hexahydrate)
Appearancepale yellow solid (anhydrous)

cream-coloured solid (hexahydrate)

Density 4.46 g/cm3 (anhydrous)

2.383 g/cm3 (hexahydrate)

Melting point 682 °C (1,260 °F; 955 K)
Boiling point decomposes
92.4 g/100 mL (10 °C)
Structure
hexagonal, hP8
P63/m, No. 176
Tricapped trigonal prismatic
(nine-coordinate)
Hazards
Occupational safety and health (OHS/OSH):
Main hazards
Irritant
GHS labelling:
GHS-pictogram-exclam.svg
Warning
H315, H319
P264, P280, P302+P352, P305+P351+P338, P321, P332+P313, P337+P313, P362
Related compounds
Other anions
Samarium(III) fluoride
Samarium(III) bromide
Samarium(III) oxide
Other cations
Samarium(II) chloride
Promethium(III) chloride
Europium(III) chloride
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
X mark.svgN  verify  (what is  Yes check.svgYX mark.svgN ?)

Samarium(III) chloride, also known as samarium trichloride, is an inorganic compound of samarium and chloride. It is a pale yellow salt that rapidly absorbs water to form a hexahydrate, SmCl3.6H2O. [1] The compound has few practical applications but is used in laboratories for research on new compounds of samarium.

Contents

Structure

Like several related chlorides of the lanthanides and actinides, SmCl3 crystallises in the UCl3 motif. The Sm3+ centres are nine-coordinate, occupying trigonal prismatic sites with additional chloride ligands occupying the three square faces.

Preparation and reactions

SmCl3 is prepared by the "ammonium chloride" route, which involves the initial synthesis of (NH4)2[SmCl5]. This material can be prepared from the common starting materials at reaction temperatures of 230 °C from samarium oxide: [2]

10 NH4Cl + Sm2O3 → 2 (NH4)2[SmCl5] + 6 NH3 + 3 H2O

The pentachloride is then heated to 350-400 °C resulting in evolution of ammonium chloride and leaving a residue of the anhydrous trichloride:

(NH4)2[SmCl5] → 2 NH4Cl + SmCl3

It can also be prepared from samarium metal and hydrochloric acid. [3] [4]

2 Sm + 6 HCl → 2 SmCl3 + 3 H2

Aqueous solutions of samarium(III) chloride can be prepared by dissolving metallic samarium or samarium carbonate in hydrochloric acid.

Samarium(III) chloride is a moderately strong Lewis acid, which ranks as "hard" according to the HSAB concept. Aqueous solutions of samarium chloride can be used to prepare samarium trifluoride:

SmCl3 + 3 KF → SmF3 + 3 KCl

Uses

Samarium(III) chloride is used for the preparation of samarium metal, which has a variety of uses, notably in magnets. Anhydrous SmCl3 is mixed with sodium chloride or calcium chloride to give a low melting point eutectic mixture. Electrolysis of this molten salt solution gives the free metal. [5]

In laboratory

Samarium(III) chloride can also be used as a starting point for the preparation of other samarium salts. The anhydrous chloride is used to prepare organometallic compounds of samarium, such as bis(pentamethylcyclopentadienyl)alkylsamarium(III) complexes. [6]

Related Research Articles

<span class="mw-page-title-main">Cerium(III) chloride</span> Chemical compound

Cerium(III) chloride (CeCl3), also known as cerous chloride or cerium trichloride, is a compound of cerium and chlorine. It is a white hygroscopic salt; it rapidly absorbs water on exposure to moist air to form a hydrate, which appears to be of variable composition, though the heptahydrate CeCl3·7H2O is known. It is highly soluble in water, and (when anhydrous) it is soluble in ethanol and acetone.

<span class="mw-page-title-main">Praseodymium(III) chloride</span> Chemical compound

Praseodymium(III) chloride is the inorganic compound with the formula PrCl3. Like other lanthanide trichlorides, it exists both in the anhydrous and hydrated forms. It is a blue-green solid that rapidly absorbs water on exposure to moist air to form a light green heptahydrate.

Neodymium(III) chloride or neodymium trichloride is a chemical compound of neodymium and chlorine with the formula NdCl3. This anhydrous compound is a mauve-colored solid that rapidly absorbs water on exposure to air to form a purple-colored hexahydrate, NdCl3·6H2O. Neodymium(III) chloride is produced from minerals monazite and bastnäsite using a complex multistage extraction process. The chloride has several important applications as an intermediate chemical for production of neodymium metal and neodymium-based lasers and optical fibers. Other applications include a catalyst in organic synthesis and in decomposition of waste water contamination, corrosion protection of aluminium and its alloys, and fluorescent labeling of organic molecules (DNA).

<span class="mw-page-title-main">Europium(III) chloride</span> Chemical compound

Europium(III) chloride is an inorganic compound with the formula EuCl3. The anhydrous compound is a yellow solid. Being hygroscopic it rapidly absorbs water to form a white crystalline hexahydrate, EuCl3·6H2O, which is colourless. The compound is used in research.

<span class="mw-page-title-main">Dysprosium(III) chloride</span> Chemical compound

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 to an oxychloride, DyOCl.

<span class="mw-page-title-main">Chromium(III) chloride</span> Chemical compound

Chromium(III) chloride (also called chromic chloride) is an inorganic chemical compound with the chemical formula CrCl3. It forms several hydrates with the formula CrCl3·nH2O, among which are hydrates where n can be 5 (chromium(III) chloride pentahydrate CrCl3·5H2O) or 6 (chromium(III) chloride hexahydrate CrCl3·6H2O). The anhydrous compound with the formula CrCl3 are violet crystals, while the most common form of the chromium(III) chloride are the dark green crystals of hexahydrate, CrCl3·6H2O. Chromium chlorides find use as catalysts and as precursors to dyes for wool.

<span class="mw-page-title-main">Rhodium(III) chloride</span> Chemical compound

Rhodium(III) chloride refers to inorganic compounds with the formula RhCl3(H2O)n, where n varies from 0 to 3. These are diamagnetic solids featuring octahedral Rh(III) centres. Depending on the value of n, the material is either a dense brown solid or a soluble reddish salt. The soluble trihydrated (n = 3) salt is widely used to prepare compounds used in homogeneous catalysis, notably for the industrial production of acetic acid and hydroformylation.

<span class="mw-page-title-main">Terbium(III,IV) oxide</span> Chemical compound

Terbium(III,IV) oxide, occasionally called tetraterbium heptaoxide, has the formula Tb4O7, though some texts refer to it as TbO1.75. There is some debate as to whether it is a discrete compound, or simply one phase in an interstitial oxide system. Tb4O7 is one of the main commercial terbium compounds, and the only such product containing at least some Tb(IV) (terbium in the +4 oxidation state), along with the more stable Tb(III). It is produced by heating the metal oxalate, and it is used in the preparation of other terbium compounds. Terbium forms three other major oxides: Tb2O3, TbO2, and Tb6O11.

<span class="mw-page-title-main">Erbium(III) chloride</span> Chemical compound

Erbium(III) chloride is a violet solid with the formula ErCl3. It is used in the preparation of erbium metal.

<span class="mw-page-title-main">Gadolinium(III) chloride</span> Chemical compound

Gadolinium(III) chloride, also known as gadolinium trichloride, is GdCl3. It is a colorless, hygroscopic, water-soluble solid. The hexahydrate GdCl3∙6H2O is commonly encountered and is sometimes also called gadolinium trichloride. Gd3+ species are of special interest because the ion has the maximum number of unpaired spins possible, at least for known elements. With seven valence electrons and seven available f-orbitals, all seven electrons are unpaired and symmetrically arranged around the metal. The high magnetism and high symmetry combine to make Gd3+ a useful component in NMR spectroscopy and MRI.

<span class="mw-page-title-main">Yttrium(III) chloride</span> Chemical compound

Yttrium(III) chloride is an inorganic compound of yttrium and chloride. It exists in two forms, the hydrate (YCl3(H2O)6) and an anhydrous form (YCl3). Both are colourless salts that are highly soluble in water and deliquescent.

<span class="mw-page-title-main">Ytterbium(III) chloride</span> Chemical compound

Ytterbium(III) chloride (YbCl3) is an inorganic chemical compound. It reacts with NiCl2 to form a very effective catalyst for the reductive dehalogenation of aryl halides. It is poisonous if injected, and mildly toxic by ingestion. It is an experimental teratogen, known to irritate the skin and eyes.

<span class="mw-page-title-main">Lanthanum(III) chloride</span> Chemical compound

Lanthanum chloride is the inorganic compound with the formula LaCl3. It is a common salt of lanthanum which is mainly used in research. It is a white solid that is highly soluble in water and alcohols.

<span class="mw-page-title-main">Bismuth chloride</span> Chemical compound

Bismuth chloride (or butter of bismuth) is an inorganic compound with the chemical formula BiCl3. It is a covalent compound and is the common source of the Bi3+ ion. In the gas phase and in the crystal, the species adopts a pyramidal structure, in accord with VSEPR theory.

<span class="mw-page-title-main">Thulium(III) chloride</span> Chemical compound

Thulium(III) chloride or thulium trichloride is as an inorganic salt composed of thulium and chlorine with the formula TmCl3. It forms yellow crystals. Thulium(III) chloride has the YCl3 (AlCl3) layer structure with octahedral thulium ions. It has been used as a starting material for some exotic nanostructures prepared for NIR photocatalysis.

Lanthanide trichlorides are a family of inorganic compound with the formula LnCl3, where Ln stands for a lanthanide metal. The trichlorides are standard reagents in applied and academic chemistry of the lanthanides. They exist as anhydrous solids and as hydrates.

<span class="mw-page-title-main">Berkelium(III) chloride</span> Chemical compound

Berkelium(III) chloride also known as berkelium trichloride, is a chemical compound with the formula BkCl3. It is a water-soluble green salt with a melting point of 603 °C. This compound forms the hexahydrate, BkCl3·6H2O.

Manganese(III) chloride is the hypothetical inorganic compound with the formula MnCl3.

Erbium compounds are compounds containing the element erbium (Er). These compounds are usually dominated by erbium in the +3 oxidation state, although the +2, +1 and 0 oxidation states have also been reported.

Lanthanide chlorides are a group of chemical compounds that can form between a lanthanide element and chlorine. The lanthanides in these compounds are usually in the +2 and +3 oxidation states, although compounds with lanthanides in lower oxidation states exist.

References

  1. ↑ F. T. Edelmann, P. Poremba (1997). W. A. Herrmann (ed.). Synthetic Methods of Organometallic and Inorganic Chemistry. Vol. 6. Stuttgart: Georg Thieme Verlag.
  2. ↑ Meyer, G. (1989). "The Ammonium Chloride Route to Anhydrous Rare Earth Chlorides—The Example of Ycl 3". The Ammonium Chloride Route to Anhydrous Rare Earth Chlorides-The Example of YCl3. Inorganic Syntheses. Vol. 25. pp. 146–150. doi:10.1002/9780470132562.ch35. ISBN   978-0-470-13256-2.
  3. ↑ L. F. Druding, J. D. Corbett (1961). "Lower Oxidation States of the Lanthanides. Neodymium(II) Chloride and Iodide". J. Am. Chem. Soc. 83 (11): 2462–2467. doi:10.1021/ja01472a010.
  4. ↑ J. D. Corbett (1973). "Reduced Halides of the Rare Earth Elements". Rev. Chim. Minérale . 10: 239.
  5. ↑ Greenwood, Norman N.; Earnshaw, Alan (1984). Chemistry of the Elements. Oxford: Pergamon Press. ISBN   978-0-08-022057-4.
  6. ↑ G. A. Molander, E. D. Dowdy (1999). Shu Kobayashi (ed.). Lanthanides: Chemistry and Use in Organic Synthesis. Berlin: Springer-Verlag. pp.  119–154. ISBN   3-540-64526-8.
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