From Handwiki | Names | |
|---|---|
| IUPAC name
Iron(III) iodide
| |
| Other names
Ferric iodide
| |
| Identifiers | |
3D model (JSmol)
|
|
| ChemSpider | |
PubChem CID
|
|
CompTox Dashboard (EPA)
|
|
| |
| |
| Properties | |
| FeI3 | |
| Molar mass | 436.56 g/mol |
| Appearance | Black solid |
| decomposes | |
| Solubility | sparingly soluble in dichloromethane |
| Related compounds | |
Other anions
|
FeF3, FeCl3, FeBr3 |
Other cations
|
ScI3, TiI3, VI3, MoI3, WI3, RhI3, BiI3 |
Related compounds
|
FeI2 |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
| Infobox references | |
Iron(III) iodide is an inorganic compound with the chemical formula FeI3. It is a thermodynamically unstable compound that is difficult to prepare. Nevertheless, iron(III) iodide has been synthesised in small quantities in the absence of air and water.[1]
Iron(III) and iodide tend to undergo a redox reaction[1] in which Fe3+ is reduced to Fe2+ and I− is oxidised to I2. This reaction can be avoided and iron(III) iodide can be synthesised by a photochemical reaction. Iron pentacarbonyl reacts with excess iodine in hexane under argon, releasing carbon monoxide and forming the complex diiodotetracarbonyliron(II), Fe(CO)4I2, as a light red solution.[1][2]
This complex then undergoes oxidative photodecarbonylation at −20 °C in the presence of further iodine and actinic light. A black film of FeI3 is deposited as further carbon monoxide is evolved.[1][2]
Iron(III) iodide is prone to light-induced decomposition to iron(II) iodide and iodine.[2][3][4]
Donor solvents such as tetrahydrofuran, acetonitrile, pyridine and water also promote this reaction: iron(III) iodide is extremely hygroscopic. It is sparingly soluble in dichloromethane. It reacts with iodide to form the tetraiodoferrate(III) ion.[2]
Iron(III) iodide undergoes ligand exchange or metathesis with certain alkyl chlorides to reversibly form iron(III) chloride and the corresponding alkyl iodides.[2]
Adducts of FeI3 are well known. An orange complex can be prepared from FeI2 and I2 in the presence of thiourea.[5][6] Iron powder reacts with iodine-containing proligands to also give adducts of ferric iodide.[7]
| HI | He | ||||||||||||||||
| LiI | BeI2 | BI3 | CI4 | NI3 | I2O4, I2O5, I4O9 |
IF, IF3, IF5, IF7 |
Ne | ||||||||||
| NaI | MgI2 | AlI3 | SiI4 | PI3, P2I4 |
S | ICl, ICl3 |
Ar | ||||||||||
| KI | CaI2 | Sc | TiI4 | VI3 | CrI3 | MnI2 | FeI2 | CoI2 | NiI2 | CuI | ZnI2 | Ga2I6 | GeI2, GeI4 |
AsI3 | Se | IBr | Kr |
| RbI | SrI2 | YI3 | ZrI4 | NbI5 | Mo | Tc | Ru | Rh | Pd | AgI | CdI2 | InI3 | SnI4, SnI2 |
SbI3 | TeI4 | I | Xe |
| CsI | BaI2 | HfI4 | TaI5 | W | Re | Os | Ir | Pt | AuI | Hg2I2, HgI2 |
TlI | PbI2 | BiI3 | Po | AtI | Rn | |
| Fr | RaI2 | Rf | Db | Sg | Bh | Hs | Mt | Ds | Rg | Cn | Nh | Fl | Mc | Lv | Ts | Og | |
| ↓ | |||||||||||||||||
| La | Ce | Pr | Nd | Pm | SmI2 | Eu | Gd | TbI3 | Dy | Ho | Er | Tm | Yb | Lu | |||
| Ac | ThI4 | Pa | UI3, UI4 |
Np | Pu | Am | Cm | Bk | Cf | EsI3 | Fm | Md | No | Lr | |||
![]() |
Categories: [Iron(III) compounds] [Iodides]