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Bis[(pentamethylcyclopentadienyl)dichloro-rhodium]
[CAS# 12354-85-7]

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Identification
Classification Organic raw materials >> Organometallic compound >> Organic rhodium
Name Bis[(pentamethylcyclopentadienyl)dichloro-rhodium]
Synonyms Dichloro(pentamethylcyclopentadienyl)rhodium(III) dimer; Pentamethylcyclopentadienylrhodium(III) chloride dimer
Molecular Structure CAS # 12354-85-7, Bis[(pentamethylcyclopentadienyl)dichloro-rhodium], Dichloro(pentamethylcyclopentadienyl)rhodium(III) dimer, Pentamethylcyclopentadienylrhodium(III) chloride dimer
Molecular Formula C20H30Cl4Rh2
Molecular Weight 618.08
CAS Registry Number 12354-85-7
EC Number 625-704-0
SMILES Cl[Rh]Cl.Cl[Rh]Cl.C[C]1[C](C)[C](C)[C](C)[C]1C.C[C]2[C](C)[C](C)[C](C)[C]2C
Safety Data
Hazard Symbols symbol   GHS07 Warning    Details
Hazard Statements H302+H312+H332-H315-H319    Details
Precautionary Statements P501-P261-P270-P271-P264-P280-P337+P313-P305+P351+P338-P362+P364-P332+P313-P301+P312+P330-P302+P352+P312-P304+P340+P312    Details
Hazard Classification
up    Details
HazardClassCategory CodeHazard Statement
Skin irritationSkin Irrit.2H315
Acute toxicityAcute Tox.4H332
Acute toxicityAcute Tox.4H312
Eye irritationEye Irrit.2H319
Acute toxicityAcute Tox.4H302
Specific target organ toxicity - single exposureSTOT SE3H335
Respiratory sensitizationResp. Sens.1H334
Substances or mixtures corrosive to metalsMet. Corr.1H290
Chronic hazardous to the aquatic environmentAquatic Chronic4H413
Eye irritationEye Irrit.2AH319
SDS Available
up Discovory and Applicatios
Bis\[(pentamethylcyclopentadienyl)dichloro-rhodium] is an organorhodium complex with the formula \[(C5Me5)RhCl2]2, where C5Me5 represents the pentamethylcyclopentadienyl (Cp\*) ligand. The complex consists of two rhodium(III) centers, each coordinated by one η5-pentamethylcyclopentadienyl ligand and two chloride ligands. These two rhodium units are bridged via chloride ligands, forming a dimeric structure. The compound commonly appears as a red-orange crystalline solid and is soluble in various organic solvents such as dichloromethane and chloroform.

This compound was characterized during studies of cyclopentadienyl transition metal complexes in the late 20th century, when the pentamethylcyclopentadienyl ligand was found to provide enhanced steric protection and electron donation compared to the unsubstituted cyclopentadienyl ring. Structural analyses, including X-ray crystallography, confirmed the dimeric arrangement and octahedral coordination geometry around each rhodium center, with the Cp\* ligand occupying one face of the octahedron and chlorides completing the coordination sphere.

Bis\[(pentamethylcyclopentadienyl)dichloro-rhodium] is typically synthesized by reacting rhodium trichloride hydrate with pentamethylcyclopentadiene under reflux conditions, sometimes with added base to facilitate complex formation. The product can be isolated by crystallization or filtration from the reaction mixture.

This complex serves as an important precursor in the preparation of rhodium-based catalysts and organometallic derivatives. The chloride ligands can be substituted by various ligands, including phosphines, nitrogen donors, or carbenes, leading to monomeric or polynuclear species with tailored catalytic properties. Such derivatives find applications in homogeneous catalysis, including hydrogenation, hydroformylation, and C–H activation reactions.

The compound’s stability and solubility also make it useful in mechanistic studies and as a building block for advanced organometallic architectures.

Handling of bis\[(pentamethylcyclopentadienyl)dichloro-rhodium] requires care due to the toxicity of rhodium compounds and potential irritant effects. Appropriate protective equipment and good laboratory practices should be observed.

In summary, bis\[(pentamethylcyclopentadienyl)dichloro-rhodium] is a stable dimeric rhodium(III) complex featuring Cp\* and chloride ligands. It is widely used as a versatile precursor in organometallic synthesis and catalysis because of its ligand exchangeability and robust structural properties.
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