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Chloro(1,5-cyclooctadiene)rhodium(I) dimer

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Chloro(1,5-cyclooctadiene)rhodium(I) dimer Basic information

Product Name:
Chloro(1,5-cyclooctadiene)rhodium(I) dimer
Synonyms:
  • Bis(1,5-cyclohexadiene)-mu,mu'-dichlorodirhodium
  • Bis(cycloocta-1,5-diene)dichlorodirhodium
  • Chloro(1,5-cyclooctadiene)rhodium dimer
  • Dichloro-bis-1,5-cyclooctadiene dirhodium
  • Di-mu-chlorobis(1,5-cyclooctadiene)dirhodium
  • di-mu-chlorobis[(1,2,5,6-eta)-1,5-cyclooctadiene]di-rhodiu
  • Rhodium 1,5-cyclooctadiene chloride dimer
  • Rhodium chloro(cycloocta-1,5-diene) dimer
CAS:
12092-47-6
MF:
C16H24Cl2Rh2
MW:
493.08
EINECS:
235-157-6
Product Categories:
  • Morpholines/Thiomorpholines ,Isoxazoles
  • Rh
  • Rh (Rhodium) Compounds
  • Catalysts for Organic Synthesis
  • Classes of Metal Compounds
  • Homogeneous Catalysts
  • Metal Complexes
  • Synthetic Organic Chemistry
  • Transition Metal Compounds
  • organometallic complexes
Mol File:
12092-47-6.mol
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Chloro(1,5-cyclooctadiene)rhodium(I) dimer Chemical Properties

Melting point:
243 °C (dec.) (lit.)
Density 
1.94[at 20℃]
vapor pressure 
0Pa at 25℃
storage temp. 
Inert atmosphere,Room Temperature
solubility 
Soluble in chloroform, dichloromethane, and methanol. Sparingly soluble in most common solvents.
form 
Crystals or Crystalline Powder
color 
Orange to orange-brown
Water Solubility 
1.56g/L at 20℃
Sensitive 
Air Sensitive & Hygroscopic
Exposure limits
ACGIH: TWA 0.01 mg/m3; TWA 1 mg/m3
NIOSH: IDLH 2 mg/m3; IDLH 100 mg/m3; TWA 0.001 mg/m3; TWA 0.1 mg/m3
Stability:
hygroscopic
LogP
3.16 at 20℃
NIST Chemistry Reference
Bis(1,5-cyclooctadienerhodium chloride)(12092-47-6)
EPA Substance Registry System
Rhodium, di-.mu.-chlorobis[(1,2,5,6-.eta.)-1,5-cyclooctadiene]di- (12092-47-6)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-37/39
WGK Germany 
3
3
TSCA 
Yes
HS Code 
28439000

MSDS

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Chloro(1,5-cyclooctadiene)rhodium(I) dimer Usage And Synthesis

Reaction

  1. Catalyst for coupling 1,3-dienes with activate methylene compounds.
  2. Rhodium source for various asymmetric hydrogenation systems and asymmetric hydrosilylation of ketones.
  3. Rhodium source for asymmetric reductive aldol reaction.
  4. Cis-hydroboration of terminal alkynes.
  5. Rhodium source for [5 + 2] additions.
  6. Highly enantioselective for [2+2+2] carbocyclization reactions.
  7. Enantioselective hydroboration of cyclopropenes.

Chemical Properties

orange crystals

Uses

It is a widely used precursor to homogeneous catalysts. This is a chiral catalyst capable of asymmetrically hydrogenating certain prochiral alkenes. Chloro(1,5-cyclooctadiene)rhodium(I) dimer is also used in the synthesis of other metal ligands for use in catalysis.

Uses

Chloro(1,5-cyclooctadiene)rhodium(I) dimer ([Rh(COD)Cl]2) can be:

  • Employed for the synthesis of rhodium complex of heterocyclic carbenes (NHCs).
  • Modified and coated on the surface of ferrite magnetic nanoparticles for catalyzing hydroformylation reaction of olefins.
  • Used for the synthesis of triple-layer structure to be used as a ring-opening polymerization catalyst.
  • As an effective catalyst for dehydrogenation of amine-borane adducts (hydrogen storage materials) such as ammonia-borane.

General Description

This product has been enhanced for catalytic efficiency.

Flammability and Explosibility

Not classified

Chloro(1,5-cyclooctadiene)rhodium(I) dimer Preparation Products And Raw materials

Raw materials

Chloro(1,5-cyclooctadiene)rhodium(I) dimerSupplier

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