Chlorobis(ethylene)rhodium dimer

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Chlorobis(ethylene)rhodium dimer
Rh2Cl2 C2H4 4.svg
Identifiers
  • 12081-16-2
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.031.938 Edit this at Wikidata
EC Number
  • 235-145-0
  • InChI=1S/4C2H4.2ClH.2Rh/c4*1-2;;;;/h4*1-2H2;2*1H;;/p-2
    Key: QPOCZCJMFQWGSP-UHFFFAOYSA-L
  • C=C.C=C.C=C.C=C.[Cl-].[Cl-].[Rh].[Rh]
Properties
C8H16Cl2Rh2
Molar mass 388.93
Appearance red solid
Hazards
GHS labelling:
GHS07: Exclamation mark
Signal word
 Warning
H315, H319
P264, P280, P302+P352, P305+P351+P338, P321, P332+P313, P337+P313, P362
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references

Chlorobis(ethylene)rhodium dimer is an organorhodium compound with the formula Rh2Cl2(C2H4)4. It is a red-orange solid that is soluble in nonpolar organic solvents. The molecule consists of two bridging chloride ligands and four ethylene ligands. The ethylene ligands are labile and readily displaced even by other alkenes. A variety of homogeneous catalysts have been prepared from this complex.[1][2]

Preparation and reactions[]

The complex is prepared by treating an aqueous methanolic solution of hydrated rhodium trichloride with ethylene at room temperature. Rh(III) is reduced with oxidation of ethylene to acetaldehyde:

2 RhCl3(H2O)3 + 6 C2H4 → Rh2Cl2(C2H4)4 + 2 CH3CHO + 4 HCl + 4 H2O

Reflecting the lability of its ligands, the complex does not tolerate recrystallization.[3]

The complex reacts slowly with water to give acetaldehyde. With HCl, it gives RhCl2(C2H2)2−. Rh2Cl2(C2H4)4 catalyzes the dimerization of ethylene to 1-butene.

Carbonylation affords rhodium carbonyl chloride. Treatment with acetylacetone and aqueous KOH gives Rh(acac)(C2H4)2.

References[]

  1. ^ Hayashi, Tamio; Takahashi, Makoto; Takaya, Yoshiaki; Ogasawara, Masamichi "Catalytic Cycle of Rhodium-Catalyzed Asymmetric 1,4-Addition of Organoboronic Acids. Arylrhodium, Oxa-π-allylrhodium, and Hydroxorhodium Intermediates" Journal of the American Chemical Society 2002, vol. 124, pp. 5052-5058.doi:10.1021/ja012711i
  2. ^ Neely, Jamie M. (2014). "chlorobis(ethylene)rhodium(I) dimer". e-EROS Encyclopedia of Reagents for Organic Synthesis: 1-6. doi:10.1002/047084289X.rn01715. }}
  3. ^ Richard Cramer "Di-μ-chlorotetrakis(ethylene)dirhodium(I), 2,4-pentanedionatobis(ethylene)rhodium(I), and di-μ-chlorotetracarbonyldirhodium(I)" Inorganic Syntheses 1974, vol. 15, pp. 14-18.. doi:10.1002/9780470132463.ch4
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