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Iron(III) iodide

From Wikipedia, the free encyclopedia
Iron(III) iodide
Names
IUPAC name
Iron(III) iodide
Other names
Ferric iodide
Identifiers
3D model (JSmol)
ChemSpider
  • InChI=1S/Fe.3HI/h;3*1H/q+3;;;/p-3
    Key: HEJPGFRXUXOTGM-UHFFFAOYSA-K
  • [Fe+3].[I-].[I-].[I-]
Properties
FeI3
Molar mass436.56 g/mol
AppearanceBlack solid
decomposes
Solubilitysparingly soluble indichloromethane
Related compounds
Otheranions
FeF3,FeCl3,FeBr3
Othercations
ScI3,TiI3,VI3,MoI3,WI3,RhI3,BiI3
Related compounds
FeI2
Except where otherwise noted, data are given for materials in theirstandard state (at 25 °C [77 °F], 100 kPa).
Chemical compound

Iron(III) iodide is aninorganic compound with thechemical formula FeI3. It is athermodynamically 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]

Preparation

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Iron(III) and iodide tend to undergo aredox 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 aphotochemical reaction.Iron pentacarbonyl reacts with excessiodine in hexane under argon, releasingcarbon monoxide and forming the complexdiiodotetracarbonyliron(II), Fe(CO)4I2, as a light red solution.[1][2]

Fe(CO)5 + I2 → Fe(CO)4I2 + CO

This complex then undergoes oxidative photodecarbonylation at −20 °C in the presence of further iodine andactinic light. A black film of FeI3 is deposited as further carbon monoxide is evolved.[1][2]

Fe(CO)4I2 + ½I2 + → FeI3 + 4CO

Reactivity

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Iron(III) iodide is prone tolight-induced decomposition toiron(II) iodide and iodine.[2][3][4]

FeI3 + → FeI2 + ½I2

Donor solvents such astetrahydrofuran,acetonitrile,pyridine andwater also promote this reaction: iron(III) iodide is extremelyhygroscopic. It is sparingly soluble indichloromethane. It reacts with iodide to form the tetraiodoferrate(III) ion.[2]

FeI3 + I → FeI4

Iron(III) iodide undergoesligand exchange ormetathesis with certainalkyl chlorides toreversibly formiron(III) chloride and the correspondingalkyl iodides.[2]

FeI3 + 3 RCl ⇌ FeCl3 + 3 RI

Adducts of FeI3 are well known. An orange complex can be prepared from FeI2 and I2 in the presence ofthiourea.[5][6] Iron powder reacts with iodine-containing proligands to also give adducts of ferric iodide.[7]

See also

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References

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  1. ^abcdGreenwood, Norman N.; Earnshaw, Alan (1997).Chemistry of the Elements (2nd ed.).Butterworth-Heinemann. pp. 1083–1084.doi:10.1016/C2009-0-30414-6.ISBN 978-0-08-037941-8.
  2. ^abcdeYoon, K. B.; Kochi, J. K. (1990). "Ferric iodide as a nonexistent compound".Inorg. Chem.29 (4):869–874.doi:10.1021/ic00329a058.
  3. ^Šima, Jozef; Brezová, Vlasta (2002). "Photochemistry of iodo iron(III) complexes".Coord. Chem. Rev.229 (1–2):27–35.doi:10.1016/S0010-8545(02)00018-8.
  4. ^Housecroft, C. E.; Sharpe, A. G. (2008).Inorganic Chemistry (3rd ed.). Prentice Hall. p. 716.ISBN 978-0-13-175553-6.
  5. ^Pohl, Siegfried; Bierbach, Ulrich; Saak, Wolfgang (1989). "FeI3SC(NMe2)2, a Neutral Thiourea Complex of Iron(III) Iodide".Angew. Chem. Int. Ed.28 (6):776–777.doi:10.1002/anie.198907761.
  6. ^Pohl, S.; Opitz, U.; Saak, W.; Haase, D. (1993). "Komplexe von FeI2 und FeI3 mit Tetramethylharnstoff".Z. Anorg. Allg. Chem.619 (3):608–612.doi:10.1002/zaac.19936190329.
  7. ^Barnes, Nicholas A.; Godfrey, Stephen M.; Ho, Nicholas; McAuliffe, Charles A.; Pritchard, Robin G. (2013). "Facile synthesis of a rare example of an iron(III) iodide complex, [FeI3(AsMe3)2], from the reaction of Me3AsI2 with unactivated iron powder".Polyhedron.55:67–72.doi:10.1016/j.poly.2013.02.066.
Fe(−II)
Fe(0)
Organoiron(0) compounds
Fe(I)
Organoiron(I) compounds
Fe(0,II)
Fe(II)
Organoiron(II) compounds
Fe(0,III)
Fe(II,III)
Fe(III)
Organoiron(III) compounds
Fe(IV)
Fe(VI)
Purported
Salts and covalent derivatives of theiodide ion
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