Pentamethylcyclopentadienyl)iridium(III) chloride dimer

Catsyn offer gram to tons of Pentamethylcyclopentadienyl)iridium(III) chloride dimer | CAS 12354-84-6, its formula is 2C10H15.2Cl2Ir, molecular weight is 796.709g/mol and the purity is usually 98% Min..

Synonyms : (PENTAMETHYLCYCLOPENTADIENYL)IRIDIUM(III) CHLORIDE DIMER;(PENTAMETHYLCYCLOPENTADIENYL)IRIDIUM(III) DICHLORIDE DIMER;DICHLORO(PENTAMETHYLCYCLOPENTADIENYL)IRIDIUM(III);DICHLORO(PENTAMETHYLCYCLOPENTADIENYL)IRIDIUM(III) DIMER;Pentamethylcyclopentadienyl)iridium(III) chloride dimer

This substance (CAS No.: 12354-84-6), used as a catalyst and ligand, typically contains specific functional groups or metal binding sites in its molecular structure, endowing it with unique physicochemical properties. Its electronic effects can be modulated by the electron-withdrawing or electron-donating characteristics of substituents, thereby affecting the distribution of molecular orbital energy levels, especially the band gap between the highest occupied molecular orbital (HOMO) and the lowest unoccupied molecular orbital (LUMO), which is crucial for electron transfer processes in catalytic reactions. The presence of conjugated systems (such as aromatic rings or π-conjugated chains) in the molecule can enhance electron delocalization, improve stability, and lower the activation energy of the reaction. Its catalytic activity often exhibits high selectivity and efficiency for specific reactions (such as oxidation, reduction, or coupling reactions), stemming from its ability to form stable intermediates with the metal center through coordination, optimizing the reaction pathway. As a ligand, its steric hindrance and electron-donating characteristics can finely regulate the geometry and electronic state of the metal center, thus affecting the rate of the catalytic cycle and the product distribution. In application fields, this substance is widely used as a catalyst or ligand in organic synthesis, homogeneous catalysis, and materials science. In organic synthesis, it can efficiently catalyze cross-coupling reactions (such as the Suzuki-Miyaura reaction), achieving precise construction of carbon-carbon bonds and significantly improving the synthesis efficiency of pharmaceutical intermediates and fine chemicals. In homogeneous catalysis, its coordination complexes with transition metals (such as palladium and ruthenium) can catalyze asymmetric hydrogenation reactions, generating chiral molecules with high enantioselectivity, meeting the stringent optical purity requirements of the pharmaceutical industry. In materials science, as a ligand, it can regulate the structure of metal-organic frameworks (MOFs) or coordination polymers, optimizing their performance in gas storage, catalysis, or optoelectronics. Its core value lies in achieving precise control of catalytic performance through molecular design, reducing energy consumption and waste generation in industrial processes, while promoting the green synthesis of high-value-added chemicals and advanced materials, which is of significant strategic importance to the sustainable development of the chemical industry.