Chloro(1,5-cyclooctadiene)iridium(I) dimer CAS: 12112-67-3
Catalog Number | XD94449 |
Product Name | Chloro(1,5-cyclooctadiene)iridium(I) dimer |
CAS | 12112-67-3 |
Molecular Formula | C16H24Cl2Ir2 |
Molecular Weight | 671.7 |
Storage Details | Ambient |
Product Specification
Appearance | White powder |
Assay | 99% min |
Chloro(1,5-cyclooctadiene)iridium(I) dimer, also known as Ir(cod)Cl dimer, is a complex organometallic compound consisting of two iridium atoms coordinated with chloride ions and 1,5-cyclooctadiene ligands. This compound finds extensive use as a versatile catalyst in various organic transformations.One of the primary applications of Ir(cod)Cl dimer is in homogeneous catalysis, specifically in C-H activation reactions. The presence of the Ir(I) center and the cyclooctadiene ligands allows for efficient activation of C-H bonds, making it suitable for various transformations such as functionalization, cycloadditions, and cross-coupling reactions. For instance, Ir(cod)Cl dimer can catalyze the direct arylation of C-H bonds, enabling the synthesis of complex organic molecules with high efficiency and selectivity.Additionally, Ir(cod)Cl dimer is a valuable catalyst in the field of hydrofunctionalization reactions. It can promote the addition of nucleophiles, such as amines or alcohols, to unsaturated bonds, leading to the formation of valuable functionalized compounds. This capability has broad utility in the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals.Furthermore, Ir(cod)Cl dimer is utilized in the catalytic synthesis of annulated compounds. By taking advantage of the reactivity of the cyclooctadiene ligand, this complex can coordinate with various unsaturated substrates, enabling the formation of complex cyclic structures. This application has implications in the production of natural products and other structurally intricate organic molecules.Ir(cod)Cl dimer is also employed as a catalyst in the hydrosilylation reaction. This transformation involves the addition of silanes to unsaturated bonds, leading to the formation of silicon-containing compounds. The unique reactivity of Ir(cod)Cl dimer allows for efficient catalysis of this reaction, enabling the synthesis of organosilicon compounds that find applications in materials science and polymer chemistry.Moreover, Ir(cod)Cl dimer serves as a precursor for the synthesis of other iridium-based catalysts. By modifying the ligands coordinated to the iridium center, the reactivity and selectivity of the resulting catalysts can be tailored for specific organic transformations. This versatility makes Ir(cod)Cl dimer an essential building block in catalyst development.In summary, Chloro(1,5-cyclooctadiene)iridium(I) dimer (Ir(cod)Cl dimer) is a highly versatile catalyst used in various organic transformations. Its ability to activate C-H bonds, catalyze hydrofunctionalization reactions, promote annulation processes, and facilitate hydrosilylation reactions make it a valuable tool in the synthesis of complex organic molecules. Additionally, it serves as a precursor for the development of other iridium-based catalysts, further expanding its application in homogeneous catalysis.