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Carbonylbis(triphenylphosphine)rhodium(I) chloride

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Carbonylbis(triphenylphosphine)rhodium(I) chloride Basic information

Product Name:
Carbonylbis(triphenylphosphine)rhodium(I) chloride
Synonyms:
  • RHODIUM-BIS(TRIPHENYLPHOSPHINE) CARBONYL CHLORIDE
  • TRANS-BIS(TRIPHENYLPHOSPHINE)RHODIUM(I) CARBONYL CHLORIDE
  • CARBONYLBIS(TRIPHENYLPHOSPHINE)RHODIUM(1) CHLORIDE
  • CARBONYLBIS(TRIPHENYLPHOSPHINE)RHODIUM(I) CHLORIDE
  • CARBONYLCHLOROBIS(TRIPHENYLPHOSPHINE)RHODIUM(I)
  • CHLOROCARBONYLBIS(TRIPHENYLPHOSPHINE)RHODIUM (I)
  • BIS(TRIPHENYLPHOSPHINE)RHODIUM(I) CARBONYL CHLORIDE
  • BIS(TRIPHENYLPHOSPHINE)CARBONYLRHODIUM(I) CHLORIDE
CAS:
13938-94-8
MF:
C37H30ClOP2Rh
MW:
690.94
EINECS:
237-712-8
Product Categories:
  • metal carbonyl complexes
  • Rh
  • Catalysts for Organic Synthesis
  • Classes of Metal Compounds
  • Homogeneous Catalysts
  • chemical reaction,pharm,electronic,materials
  • Metal Compounds
  • Metal Complexes
  • Rh (Rhodium) Compounds
  • Synthetic Organic Chemistry
  • Transition Metal Compounds
Mol File:
13938-94-8.mol
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Carbonylbis(triphenylphosphine)rhodium(I) chloride Chemical Properties

Melting point:
224-227 °C (dec.)(lit.)
storage temp. 
Inert atmosphere,Room Temperature
solubility 
Soluble in acetone, chloroform, ethanol
form 
crystal
color 
yellow
BRN 
4618896
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
CAS DataBase Reference
13938-94-8(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xn,T
Risk Statements 
20/21/22
Safety Statements 
22-24/25
WGK Germany 
3
HS Code 
28439090

MSDS

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Carbonylbis(triphenylphosphine)rhodium(I) chloride Usage And Synthesis

Chemical Properties

yellow crystals

Uses

Used for cyclometallation.

Synthesis

To a solution of RhCl3.3H2O (2 g, 7.6 mmol) in 70 mL of absolute ethanol is slowly added triphenylphosphine (7.2 g, 2.75 mmol) in 300 mL of boiling absolute ethanol. The solution becomes clear within 5 min, at which point sufficient (10-20 mL) 37% formaldehyde solution is added, causing the red solution to become pale yellow. After several minutes, yellow microcrystals precipitate. Upon cooling, the resulting crystals are washed with ethanol and diethyl ether, dried (4.5 g, 85%) and recrystallized from hot toluene.

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