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hexacarbonylchromium (13007-92-6)

Identification
Name:hexacarbonylchromium
Synonyms:Chromiumcarbonyl (Cr(CO)6) (8CI); Chromium carbonyl; Chromium hexacarbonyl;Hexacarbonylchromium
CAS:13007-92-6
EINECS: 235-852-4
Molecular Formula: C6CrO6
Molecular Weight: 220.06
InChI: InChI=1/6CO.Cr/c6*1-2;
Molecular Structure: (C6CrO6) Chromiumcarbonyl (Cr(CO)6) (8CI); Chromium carbonyl; Chromium hexacarbonyl;Hexacarbonylchromium
Properties
Transport:UN 3466
Flash Point: °C
Density:1.77
Stability:Stable. Incompatible with strong oxidizing agents.
Water Solubility:insoluble
Solubility:insoluble
Appearance:white crystals or powder
Specification:

 Hexacarbonylchromium (13007-92-6) 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.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.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.

Report:

IARC Cancer Review: Animal Inadequate Evidence IMEMDT    IARC Monographs on the Evaluation of Carcinogenic Risk of Chemicals to Man . 23 , 1980,p. 205.(World Health Organization, Internation Agency for Research on Cancer,Lyon, France.: ) (Single copies can be ordered from WHO Publications Centre U.S.A., 49 Sheridan Avenue, Albany, NY 12210) ; Chromium and its compounds are on the Community Right-To-Know List. Reported in EPA TSCA Inventory.

Packinggroup: II
HS Code: 29310095
Flash Point: °C
Storage Temperature: Store in a cool, dry, well-ventilated area away from incompatible substances. Store protected from light.
Sensitive: Light Sensitive/Heat Sensitive
Usage:Substance is used in catalysts for olefin polymerization and isomerization.
Safety Data
Hazard Symbols T:Toxic N:Dangerousfortheenvironment
 

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