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Samarium(II) bromide

Samarium dibromide
Names
IUPAC name
Dibromosamarium
Identifiers
3D model (JSmol)
ChemSpider
Properties
SmBr2
Molar mass 310.17 g/mol
Appearance Brown crystals
Melting point 669 °C (1,236 °F; 942 K)
Boiling point 1,880 °C (3,420 °F; 2,150 K)
+5337.0·10−6 cm3/mol
Hazards
GHS pictograms The exclamation-mark pictogram in the Globally Harmonized System of Classification and Labelling of Chemicals (GHS)
GHS signal word Warning
H315, H319, H335
P261, P305+351+338
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references

Samarium(II) bromide is a crystalline compound with the chemical formula SmBr
2
. Samarium(II) bromide is a brown crystal at room temperature.

Samarium(II) bromide was first synthesized in 1934 by P. W. Selwood, when he reduced samarium tribromide (SmBr3) with hydrogen (H2). Kagan also synthesized it by converting samarium(III) oxide (Sm2O3) to SmBr3 and then reducing with a lithium dispersion in THF. Robert A. Flowers synthesized it by adding two equivalent of lithium bromide (LiBr) to samarium diiodide (SmI2) in tetrahydrofuran. Namy managed to synthesize it by mixing tetrabromoethane (C2H2Br4) with samarium metal, and Hilmerson found that heating the tetrabromoethane or samarium greatly improved the production of samarium(II) bromide.

Samarium(II) bromide is used as a reductant, although it is not used as commonly as samarium diiodide. This is likely due to it being soluble in fewer organic liquids, however, it is an effective reagent for pinacol homocouplings of aldehydes, ketones, and cross-coupling carbonyl compounds. Reports have shown that samarium(II) bromide is capable of selectively reducing ketones if it is in the presence of an alkyl halide.

If hexamethylphosphoramide is added to samarium(II) bromide, it will strengthen it enough that it can reduce imines to amines and alkyl chlorides to hydrocarbons. However, the addition of hexamethylphosphoramide to samarium(II) bromide that is in tetrahydrofuran will strengthen it enough that it can reduce cyclohexyl chloride to cyclohexanol, at room temperature, within two hours.


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