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Features
|
CAS Number: |
12246-51-4 |
|
Linear Formula: |
C32H56Cl2Ir2 |
|
Purity: |
>97% |
|
Form: |
Yellow-orange to brown powder |
✅ Product Description
Chlorobis(cyclooctene)iridium(I) dimer is a valuable organometallic compound containing two iridium(I) centers, each coordinated by a chloride ligand and a cyclooctene ligand. It forms a dimeric structure, which makes it an excellent starting material for the preparation of various iridium complexes and catalysts.
This compound is widely used in homogeneous catalysis, particularly in hydrogenation, hydroboration, and C–H activation reactions. Due to its high reactivity and ligand substitution potential, it is a key precursor in the development of phosphine- and carbene-based iridium catalysts for industrial and academic applications.
🔹 Features & Properties
📌 Molecular Formula: C₃₂H₅₆Cl₂Ir₂
📌 Molecular Weight: ~1072.1 g/mol
📌 Appearance: Yellow-orange to brown crystalline powder
📌 Purity: >97%
📌 Solubility: Soluble in organic solvents such as dichloromethane, toluene, and THF
📌 Stability: Air-stable as a solid, sensitive to light and moisture in solution
📌 Structure: Dimeric with bridging chloride ligands
🚀 Applications & Related Industries
✅ Catalyst Precursor: Foundation for a wide range of Ir(I) complexes
✅ Hydrogenation Reactions: Efficient in selective hydrogenations
✅ C–H Activation Chemistry: Used in the synthesis of novel catalytic systems
✅ Organometallic Synthesis: Intermediate for functionalized iridium complexes
✅ Research & Development: In high-performance catalysis and coordination chemistry
📖 Synonyms
Bis(μ-chloro)bis(cyclooctene)diiridium(I)
Chloro(cyclooctene)iridium(I) dimer
(COD)IrCl dimer precursor
⚠ Health & Safety Information
⚠ Hazard Statements: May cause irritation to eyes, skin, or respiratory tract
⚠ Avoid inhalation of dust and contact with skin
Use with protective clothing, gloves, and safety goggles
Store in airtight containers in a cool, dry, and dark location
Handle under inert atmosphere for extended shelf life
🏭 Production Method & Equipment
Synthesized through the controlled reaction of iridium trichloride hydrate with cyclooctene in a suitable organic solvent under an inert gas atmosphere. The product is purified by crystallization or vacuum drying under controlled temperature and light conditions to prevent degradation.
📐 Size & Customization
Available in: 100 mg, 1 g, 5 g, and larger batch quantities
Custom packaging and labeling available upon request
📋 Certifications & Quality Assurance
Conforms to ASTM, JIS, GB, EN, and BS standards
Supplied with complete documentation: COA, MSDS, and structural analysis reports
Quality controlled by NMR, elemental analysis, and spectrophotometry
Manufactured under ISO-certified quality systems
⏱ Lead Time & MOQ
Lead Time: 5–10 working days
MOQ: 100 mg (standard); 1 g (bulk orders)
💬 FAQs (Frequently Asked Questions)
Q1: What solvents are best for dissolving this compound?
A1: It dissolves well in non-polar organic solvents such as DCM, THF, and toluene.
Q2: What is its main use in catalysis?
A2: It serves as a precursor to a variety of iridium(I) catalysts used in hydrogenation and C–H activation.
Q3: How should it be stored?
A3: In a tightly sealed container under inert gas, protected from light and moisture.
🧭 How to Choose the Product
For basic synthesis, >97% purity is suitable
Choose small quantities for R&D or catalyst screening
For scale-up and advanced research, specify solvent, format (solid/powder), and packaging needs
📏 Product Standards
Conforms to ASTM, GB, JIS, EN, and BS standards
Additional industry-specific standards (e.g., REACH, RoHS) available on request
🧪 Production & Quality Control
Synthesized and purified in controlled inert-atmosphere environments
Quality tested by NMR, IR, TGA, and elemental analysis
Each batch traceable by lot number and quality audit records
📦 Shipping & Delivery Information
Supplied in amber glass vials or sealed containers
Options include lab-grade packaging or bulk shipment
Global air or courier delivery with compliant documentation
🌱 Environmental Impact & Sustainability
Precious metal recycling supported
Produced using low-solvent and environmentally conscious synthesis
Waste reduction through efficient process control
🧼 Maintenance & Care Instructions
Store under argon or nitrogen atmosphere
Avoid repeated exposure to air or light
Reseal promptly after use to maintain integrity
🧩 Differentiation Between Products
Compared with Ir(COD)Cl monomers, the dimeric form offers enhanced reactivity and is preferred in synthetic chemistry requiring rapid ligand substitution. It also shows better air-stability in its solid form compared to more labile iridium(I) complexes.
📩 Contact Us
For quotations, COA, application notes, or tailored synthesis solutions, get in touch with our professional support team.
Chemical Identifiers
|
Linear Formula |
C32H56Cl2Ir2 |
|
MDL Number |
MFCD00213465 |
|
EC No. |
N/A |
|
Pubchem CID |
N/A |
|
IUPAC Name |
N/A |
|
SMILES |
C1CCC[CH][CH]CC1.C1CCC[CH][CH]CC1.C1CCC[CH][CH]CC1.C1CCC[CH][CH]CC1.Cl[Ir].Cl[Ir] |
|
InchI Identifier |
InChI=1S/ 4C8H14.2ClH.2Ir/ c4*1-2-4-6-8-7-5-3-1;/ h4*1-2H,3-8H2;2*1H;/ q;2*+1/p-2/b4*2-1-; |
|
InchI Key |
WBRREXQCZAFSKS-XFCUKONHSA-L |
Chlorobis(cyclooctene)iridium(I) dimer Properties (Theoretical)
|
Compound Formula |
C32H56Cl2Ir2 |
|
Molecular Weight |
896.13 |
|
Appearance |
Yellow-orange to brown powder |
|
Melting Point |
160-165 °C |
|
Boiling Point |
N/A |
|
Density |
N/A |
|
Solubility in H2O |
N/A |
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Exact Mass |
N/A |
|
Monoisotopic Mass |
896.301697 |
|
Charge |
N/A |
Chlorobis(cyclooctene)iridium(I) dimer Health & Safety Information
|
Signal Word |
Warning |
|
Hazard Statements |
H315-H319-H335 |
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Hazard Codes |
Xi |
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Precautionary Statements |
P261-P280-P305+P351+P338-P304+P340-P321P332+P313-P362-P403+P233-P405-P501 |
|
Risk Codes |
36/37/38 |
|
Safety Statements |
26-37/39 |
|
RTECS Number |
N/A |
|
Transport Information |
NONH for all modes of transport |
|
WGK Germany |
3 |
|
GHS Pictograms |
GHS08 Health Hazard
|
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