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Di-μ-chloro-tetracarbonyldirhodium(I)

ALDRICH/209031 - 97%

Synonym: Rhodium carbonyl chloride(I); Rhodium(I) carbonyl chloride; Rhodium(I) dicarbonyl chloride dimer; Tetracarbonyldi-μ−chlorodirhodium(I)

CAS Number: 14523-22-9
Empirical Formula (Hill Notation): C4Cl2O4Rh2
Molecular Weight: 388.76
EC Number: 238-540-6
MDL Number: MFCD00135610
Linear Formula: [Rh(CO)2Cl]2
Product Type: Chemical

Catalog Number PKG Qty. Price Quantity
45-209031-250MG 250 mg
$189.00
1/EA
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45-209031-1G 1 g
$415.00
1/EA
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This picture is provided solely for illustration purposes. Optical properties of the actual product may deviate. Relevant product information is printed on labeled products and other accompanying or available information material. This image depicts SKU: 209031-1G

 

assay 97%
form powder
InChI 1S/4CO.2Cl.2Rh/c4*1-2;;;;/q;;;;2*+1;2*-1
InChI key ODYPMWFHWPMOKS-UHFFFAOYSA-N
mp 120-125 °C (dec.) (lit.)
Quality Level 100 
reaction suitability core: rhodium
  reagent type: catalyst
SMILES string [C-]#[O+].[C-]#[O+].[C-]#[O+].[C-]#[O+].[Cl+]1[Rh-][Cl+][Rh-]1
storage temp. 2-8°C
Application:
  • Rhodium-Catalyzed Trans-Bis-Silylation Reactions: This study explores the use of Di-μ-chloro-tetracarbonyldirhodium(I) as a catalyst in the synthesis of specialized pyridine derivatives, demonstrating potential for creating complex molecular architectures useful in drug discovery and material science (Naka & Kobayashi, 2023 ).
  • Redox behaviour of imino-β-diketonato ligands: The research investigates the coordination chemistry of Di-μ-chloro-tetracarbonyldirhodium(I) with innovative ligands, potentially opening new pathways for catalytic systems used in pharmaceutical syntheses (Ferreira, Conradie & Conradie, 2022 ).
  • Synthesis of Thiophene-Fused Siloles through Rhodium-Catalyzed Trans-Bis-Silylation: The application of Di-μ-chloro-tetracarbonyldirhodium(I) in the synthesis of thiophene-fused siloles indicates its role in advancing materials chemistry for electronic and photonic applications (Naka et al., 2024 ).
  • Kinetic Study of the Oxidative Addition Reaction between Methyl Iodide and Complexes: Utilizing UV–Vis, IR spectroscopy, this study enhances understanding of the mechanisms involved when using Di-μ-chloro-tetracarbonyldirhodium(I) in catalytic cycles, relevant to both academia and industry settings (Ferreira et al., 2022 ).
General description: Di-μ-chloro-tetracarbonyldirhodium(I) can be used as a catalyst or catalyst precursor for various organic reactions such as Pauson-Khand reaction, allylic alkylations, rearrangement of strained rings, carbonylative ring expansion, carbonylative coupling of organometallics, hydroformylation, silylformylation, and cycloaddition reactions of alkenes, alkynes, and allenes.
Packaging: 1 g in glass bottle
Packaging: 250 mg in glass bottle
RIDADR NONH for all modes of transport
WGK Germany WGK 3
Flash Point(F) Not applicable
Flash Point(C) Not applicable
Purity 97%
mp 120-125 °C (dec.) (lit.)
Storage Temp. 2-8°C
UNSPSC 12352300

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