(S)-(+)-1-[(R)-2-(Diphenylphosphino)ferrocenyl]ethyldicyclohexylphosphine ethanol adduct

Catsyn offer gram to tons of (S)-(+)-1-[(R)-2-(Diphenylphosphino)ferrocenyl]ethyldicyclohexylphosphine ethanol adduct | CAS 162291-02-3, its formula is C31H39P2.C5H5.Fe, molecular weight is 594.537g/mol and the purity is usually 98% Min..

Synonyms : (2S)-1-[(1S)-1-(DICYCLOHEXYLPHOSPHINO)ETHYL]-2-(DIPHENYLPHOSPHINO)FERROCENE;(S)-(+)-1-[(R)-2-(DIPHENYLPHOSPHINO)FERROCENYL]ETHYLDICYCLOHEXYLPHOSPHINE;(S)-(+)-1-[(R)-2-(DIPHENYLPHOSPHINO)FERROCENYL]ETHYLDICYCLOHEXYLPHOSPHINE ETHANOL ADDUCT;(S)-(R)-JOSIPHOS;(S)-1-[(RP)-2-(DIPHENYLPHOSPHINO)FERROCENYL]ETHYLDICYCLOHEXYLPHOSPHINE;FERROCENE, 1-[(1S)-1-(DICYCLOHEXYLPHOSPHINO)ETHYL]-2-(DIPHENYLPHOSPHINO)-, (2S)-;JOSIPHOS SL-J001-2

This substance (CAS No.: 162291-02-3), used as a catalyst and ligand, typically contains specific functional groups or heteroatoms (such as nitrogen, oxygen, and phosphorus) in its molecular structure. These groups bind to the central metal ion through covalent or coordinate bonds, forming stable coordination compounds. Its physicochemical properties include good solubility in specific solvents, with melting and boiling points varying depending on molecular weight and structure. Regarding electronic effects, electron-donating or electron-withdrawing groups in the ligand can significantly modulate the electron cloud density of the central metal, thus affecting its catalytic activity. In terms of energy level distribution, orbital hybridization between the ligand and the metal forms new molecular orbitals, optimizing the adsorption and activation energy barriers of the reactants. The presence of conjugated systems (such as aromatic rings or conjugated double bonds) enhances molecular stability and improves coordination ability through π-π interactions or electron delocalization effects. In terms of stability, this ligand inhibits the oxidation or hydrolysis of the metal center through steric hindrance or electronic effects, ensuring the persistence of the catalytic cycle. Its catalytic activity stems from the precise control of reaction intermediates, such as reducing transition state energy or stabilizing highly reactive species. In terms of coordination properties, this substance can form monodentate, bidentate, or multidentate coordination structures with various transition metals (such as Pd, Ni, Cu, etc.), and the catalytic selectivity can be optimized by adjusting the number of coordination teeth and spatial configuration. In application fields, this substance is widely used as a catalyst and ligand in organic synthesis, homogeneous catalysis, and materials science. Functionally, it achieves efficient construction of carbon-carbon and carbon-heteroatom bonds through the coordination metal center. For example, it acts as a key ligand to improve reaction yield and selectivity in cross-coupling reactions (such as the Suzuki and Heck reactions); in asymmetric catalysis, the chiral ligand structure can induce stereoselectivity of products, meeting the stringent requirements for optical purity in drug synthesis. Core applications cover the synthesis of pharmaceutical intermediates, polymer material preparation, and fine chemical production. For example, as a ligand in OLED material synthesis, it enables the directional preparation of high-luminescence-efficiency molecules by regulating the metal-catalyzed cyclization reaction pathway. Its industry value lies in its ability to significantly reduce energy consumption and waste generation in industrial catalytic processes, aligning with the demands of green chemistry development. Simultaneously, through ligand structure optimization, it can develop novel catalytic systems with high activity and stability, driving process upgrades and product iterations in fields such as chemical engineering, pharmaceuticals, and display technology.