Chromium carbonyl

Chembox new
Name = Chromium carbonyl
ImageFile = Cr(CO)6.png ImageSize = 150px
ImageName =
IUPACName = hexacarbonylchromium(0)
OtherNames = chromium carbonyl
Section1 = Chembox Identifiers
CASNo = 13007-92-6
RTECS = GB5075000
Section2 = Chembox Properties
Formula = C₆CrO₆
MolarMass = 220.06 g/mol
Appearance = colorless crystals
Density = 1.77 g/cm³, solid
Solubility = insoluble
Solvent = other solvents
SolubleOther = soluble in benzene, THF
MeltingPt = 150 °C (decomposition)
BoilingPt = sublimes
Section3 = Chembox Structure
Coordination = octahedral
CrystalStruct = orthrhombic
Dipole = 0 D
Section7 = Chembox Hazards
ExternalMSDS =
MainHazards = CO source
RPhrases = R22
SPhrases = S53 S36 S45
Section8 = Chembox Related
Function = compounds
OtherFunctn = V(CO)₆, Fe(CO)_5-] , CrCl₃

Chromium carbonyl, also known as chromium hexacarbonyl, is the chemical compound with the formula Cr(CO)₆. At room temperature the solid is stable to air, although it does have a high vapor pressure and sublimes readily. Cr(CO)₆ is zerovalent, meaning that Cr has a formal charge of zero, and it is called a homoleptic complex, which means that all the ligands are the same. The complex is octahedral with Cr-C and C-O distances of 1.92 and 1.17 Å, respectively. [Whitaker A.; Jeffery, J. W. “The Crystal Structure of Chromium Hexacarbonyl” Acta Crystallographica 1967, volume 23, pp. 977-984. doi|10.1107/S0365110X67004153.]

Reactions

When heated or photolyzed in tetrahydrofuran (THF) solution, Cr(CO)₆ converts to Cr(CO)₅(THF) with loss of one CO ligand. Similarly, heating a solution of Cr(CO)₆ in an aromatic solvent results in replacement of three CO ligands::Cr(CO)₆ + C₆H₅R → Cr(CO)₃(C₆H₅R) + 3 CO

Such reactions proceed particularly well with electron-rich arenes such as anisole, either as the neat reagent or using a mixture of THF and dibutyl ether, the latter to increase the boiling point of the mixture. The products adopt a "piano-stool" structure. These species are typically yellow solids, which dissolve well in common organic solvents. The arene can be liberated from the chromium with iodine or by photolysis in air. In general, substituted derivatives of Cr(CO)₆ decompose upon exposure to air.

Alkyl and aryl organolithium reagents RLi add to a carbonyl ligand to give anionic acyl complexes. [Elschenbroich, C. ”Organometallics” (2006) Wiley-VCH: Weinheim. ISBN 978-3-29390-6] These species react with alkylating agents such as Me₃O⁺ to form (OC)₅Cr=C(OMe)R, an example of a Fischer carbene. If the R group is a vinyl or an aryl group, then the resulting carbene complex can react with an acetylene to form a new benzene ring to which is bonded the chromium tricarbonyl fragment. The two acetylene carbon atoms become part of the new ring, as does a carbon from one of the carbonyl ligands. Also the three carbons from the vinyl carbene become part of the new benzene ring.

afety

In common with many of the other homoleptic metal carbonyls (e.g. nickel carbonyl and iron carbonyl), chromium hexacarbonyl is toxic and thought to be carcinogenic. Its vapor pressure is relatively high for a metal complex, 1 mm Hg ( 36 °C).

References

External links

* [http://www.npi.gov.au/database/substance-info/profiles/24.html National Pollutant Inventory - Chromium (III) and compounds fact sheet]