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(1,5-Cyclooctadiene)(methoxy)iridium(I) dimer / 1 G

Synonym: [Ir(OMe)(1,5-cod)]2, Bis(1,5-cyclooctadiene)di-μ-methoxydiiridium(I), Di-mu-methoxobis(1,5-cyclooctadiene)diiridium(I), (1Z,5Z)-cycloocta-1,5-diene;iridium;methyloxidanium, Bis(1,5-cyclooctadiene)dimethoxydiiridium,
Molecular Formula: [Ir(OCH3)(C8H12)]2
Molecular Weight: 662.86
SKU: MND-52633
CAS Number: 12148-71-9
MDL number: MFCD08459360
PubChem: 329760940
Form: crystals
Packing size: 1 G  
137.20 EUR



Safety Information


Hazard Statements

H315
H319
H335

Precautionary Statements

P280
P264
P305 + P351 + P338
P261
P271
P302 + P352

Pictograms



Properties

Signal WordWarning
Flash Point (C)Not available
Flash Point (F)Not available
Melting Point154-179 °C (D)

 Product Description

(1,5-Cyclooctadiene)(Methoxy)Iridium(I) Dimer is a coordination complex widely employed as a catalyst in various organic synthesis reactions. This organometallic compound features a cyclooctadiene ligand and a methoxy ligand coordinated to an iridium(I) center. Its unique structure imparts high reactivity, making it a valuable tool in catalyzing diverse chemical transformations.

 

Application:

Utilized as a catalyst in organic synthesis, this iridium(I) dimer facilitates key reactions, including hydrogenation and isomerization processes. Its efficacy lies in its ability to accelerate reactions under mild conditions, enhancing the efficiency of various synthetic protocols across the chemical industry.

 

 

Articles: 

- Crystal Structures of Bicyclic Organic Molecules

Publication Date: January 2000

M. Brunelli, Andy Fitch, A.J. Mora

-https://doi.org/10.4028/www.scientific.net/MSF.321-324.1092

 

- Mold Metabolites. III. The Structure of Citrinin

Publication Date: December 1, 1948

Donald J. Cram

-https://doi.org/10.1021/ja01192a078

 

- The Oxidation of Unsaturated Compounds. VI. The Effect of Oxygen Pressure on the Oxidation of α-Methylstyrene

Publication Date: May 1, 1958

Frank R. Mayo and A. A. Miller

-https://doi.org/10.1021/ja01543a031