Chlorobis(ethylene)rhodium dimer

Chlorobis(ethylene)rhodium dimer
Identifiers
CAS Number	12081-16-2;
3D model (JSmol)	Interactive image;
ChemSpider	21241609;
ECHA InfoCard	100.031.938
EC Number	235-145-0;
PubChem CID	45357812;
UNII	JF3CSZ2DN6 ;
CompTox Dashboard (EPA)	DTXSID80923566 ;
	InChI InChI=1S/4C2H4.2ClH.2Rh/c41-2;;;;/h41-2H2;2*1H;;/p-2 Key: QPOCZCJMFQWGSP-UHFFFAOYSA-L;
	SMILES C=C.C=C.C=C.C=C.[Cl-].[Cl-].[Rh].[Rh];
Properties
Chemical formula	C8H16Cl2Rh2
Molar mass	388.93
Appearance	red solid
Hazards
	GHS labelling:
Pictograms
Signal word	Warning
Hazard statements	H315, H319
Precautionary statements	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

^ 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
^ Neely, Jamie M. (2014). "chlorobis(ethylene)rhodium(I) dimer". E-EROS Encyclopedia of Reagents for Organic Synthesis: 1–6. doi:10.1002/047084289X.rn01715. ISBN 9780470842898.
^ 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

[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. ISBN 9780470842898.

[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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