Samarium(II) iodide

In samarium(II) iodide, the metal centers are seven-coordinate with a face-capped octahedral geometry.[1]

Structure of the samarium(II) iodide-tetrahydrofuran complex

In its ether adducts, samarium remains heptacoordinate with five ether and two terminal iodide ligands.[2]

Samarium iodide is easily prepared in nearly quantitative yields from samarium metal and either diiodomethane or 1,2-diiodoethane.[3] When prepared in this way, its solutions is most often used without purification of the inorganic reagent.

${\displaystyle {\begin{array}{cl}{}\\{\ce {{Sm}+ ICH2I ->[{\ce {THF}}] SmI2}}+0.5{\ce {H2C=CH2}}\\{\ce {{Sm}+ I(CH2)2I ->[{\ce {THF}}] {SmI2}+ H2C=CH2}}\\{}\end{array}}}$

()

Solid, solvent-free SmI₂ forms by high temperature decomposition of samarium(III) iodide (SmI₃).[4][5][6]

Samarium(II) iodide is a powerful reducing agent – for example it rapidly reduces water to hydrogen.[1] It is available commercially as a dark blue 0.1 M solution in THF. Although used typically in superstoichiometric amounts, catalytic applications have been described.[7]

Organic chemistry

Main article: Reductions with samarium(II) iodide

Samarium(II) iodide is a reagent for carbon-carbon bond formation, for example in a Barbier reaction (similar to the Grignard reaction) between a ketone and an alkyl iodide to form a tertiary alcohol:[8]

R¹I + R²COR³ → R¹R²C(OH)R³

Barbier reaction using SmI₂

Typical reaction conditions use SmI₂ in THF in the presence of catalytic NiI₂.

Esters react similarly (adding two R groups), but aldehydes give by-products. The reaction is convenient in that it is often very rapid (5 minutes or less in the cold). Although samarium(II) iodide is considered a powerful single-electron reducing agent, it does display remarkable chemoselectivity among functional groups. For example, sulfones and sulfoxides can be reduced to the corresponding sulfide in the presence of a variety of carbonyl-containing functionalities (such as esters, ketones, amides, aldehydes, etc.). This is presumably due to the considerably slower reaction with carbonyls as compared to sulfones and sulfoxides. Furthermore, hydrodehalogenation of halogenated hydrocarbons to the corresponding hydrocarbon compound can be achieved using samarium(II) iodide. Also, it can be monitored by the color change that occurs as the dark blue color of SmI₂ in THF discharges to a light yellow once the reaction has occurred. The picture shows the dark colour disappearing immediately upon contact with the Barbier reaction mixture.

Work-up is with dilute hydrochloric acid, and the samarium is removed as aqueous Sm³⁺.

Carbonyl compounds can also be coupled with simple alkenes to form five, six or eight membered rings.[9]

Tosyl groups can be removed from N-tosylamides almost instantaneously, using SmI₂ in conjunction with distilled water and an amine base. The reaction is even effective for deprotection of sensitive substrates such as aziridines:[10]

Removal of a tosyl group from an N-tosylamide using SmI₂

In the Markó-Lam deoxygenation, an alcohol could be almost instantaneously deoxygenated by reducing their toluate ester in presence of SmI₂.

Markó-Lam deoxygenation using SmI₂

The applications of SmI₂ have been reviewed.[11][12][13] The book Organic Synthesis Using Samarium Diiodide, published in 2009, gives a detailed overview of reactions mediated by SmI₂.[14]