(benzene)-chromium(0) tricarbonyl

(Benzene)chromium(0) tricarbonyl
IUPAC name
Other names
benzene tricarbonyl chromium, (benzene)chromium tricarbonyl, Benchrotrene, pi-benzenetricarbonylchromium
  • 12082-08-5 ☒N
3D model (JSmol)
ECHA InfoCard 100.031.939 Edit this at Wikidata
EC Number
  • 235-146-6
  • InChI=1S/C6H6.3CO.Cr/c1-2-4-6-5-3-1;3*1-2;/h1-6H;;;; checkY
  • InChI=1/C6H6.3CO.Cr/c1-2-4-6-5-3-1;3*1-2;/h1-6H;;;;
  • [Cr].[O+]#[C-].[O+]#[C-].[O+]#[C-].c1ccccc1
Molar mass 214.14 g/mol
Appearance solid yellow crystals
Melting point 163 to 166 °C (325 to 331 °F; 436 to 439 K)
Solubility THF, ether, benzene
tetrahedral, "piano stool"
Main hazards Harmful through inhalation, contact with skin, or swallowed
GHS pictograms GHS07: Harmful
GHS Signal word Warning
H302, H312, H332
P261, P264, P270, P271, P280, P301+312, P302+352, P304+312, P304+340, P312, P322, P330, P363, P501
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Infobox references

(Benzene)chromium tricarbonyl is an organometallic compound with the formula Cr(C6H6)(CO)3. This yellow crystalline solid compound is soluble in common nonpolar organic solvents. The molecule adopts a geometry known as “piano stool” because of the planar arrangement of the aryl group and the presence of three CO ligands as "legs" on the chromium-bond axis.[1]


(Benzene)tricarbonylchromium was first reported in 1957 by Fischer and Öfele, who prepared the compound by the carbonylation of bis(benzene)chromium.[2] They obtained mainly chromium carbonyl (Cr(CO)6) and traces of Cr(C6H6)(CO)3. The synthesis was optimized through the reaction of Cr(CO)6 and Cr(C6H6)2. For commercial purposes, a reaction of Cr(CO)6 and benzene is used:

Cr(CO)6 + C6H6 → Cr(C6H6)(CO)3 + 3 CO


Complexes of the type (Arene)Cr(CO)3 have been well investigated as reagents in organic synthesis..[3] The aromatic ring of (benzene)tricarbonylchromium is substantially more electrophilic than benzene itself, allowing it to undergo nucleophilic addition reactions.[4]

(Benzene)chromiumtricarbonyl electrophile nucleophilic carbonylation.png

It is also more acidic, undergoing lithiation upon treatment with n-butyllithium. The resulting organolithium compound can then be used as a nucleophile in various reactions, for example, with trimethylsilyl chloride:

(Benzene)chromiumtricarbonyl lithiation TMS.png

(Benzene)tricarbonylchromium is a useful catalyst for the hydrogenation of 1,3-dienes. The product alkene results from 1,4-addition of hydrogen. The complex does not hydrogenate isolated double bonds.


  1. ^ Gilbert T. M. Bauer C. B., Rogers R. D. (1996). "Structures of (η6-benzene dimethylacetal)- and (η6-benzene diethylacetal)chromium tricarbonyl: structural evidence for the near-electroneutrality of the dialkylacetal substituent". Journal of Chemical Crystallography. 26 (5): 355. doi:10.1007/BF01677100.
  2. ^ Fischer, Ernst Otto; Őfele, Karl. (1957). “Über Aromatenkomplexe von Metallen, XIII Benzol-Chrom-Tricarbonyl,” Chemische Berichte, 90, 2532-5. doi:10.1002/cber.19570901117.
  3. ^ E. Peter Kündig (2004). "Synthesis of Transition Metal η6-Arene Complexes". Topics Organomet Chem. 7: 3–20. doi:10.1007/b94489.
  4. ^ Herndon, James W; Laurent, Stéphane E. (2008). “(η6-Benzene)tricarbonylchromium,” in Encyclopedia of Reagents for Organic Synthesis, John Wiley & Sons, Chichester, 2008. doi:10.1002/047084289X.rb025.pub2. Article Online Posting Date: March 15, 2009