(S)-(+)-1-[(R)-2-(Dicyclohexylphosphino)ferrocenyl]ethyldicyclohexylphosphine

Catsyn offer gram to tons of (S)-(+)-1-[(R)-2-(Dicyclohexylphosphino)ferrocenyl]ethyldicyclohexylphosphine | CAS 158923-07-0, its formula is C31H51P2.C5H5.Fe, molecular weight is 606.631g/mol and the purity is usually 98% Min..

Synonyms : (S)-(+)-1-[(R)-2-(DICYCLOHEXYLPHOSPHINO)FERROCENYL] ETHYLDICYCLOHEXYLPHOSPHINE;(S)-1-[(R)-2-(DICYCLOHEXYLPHOSPHINO)FERROCENYL]-ETHYL-DICYCLOHEXYLPHOSPHINE;(S)-1-[(RP)-2-(DICYCLOHEXYLPHOSPHINO)FERROCENYL]ETHYLDICYCLOHEXYLPHOSPHINE;(S,S)-1-DICYCLOHEXYLPHOSPHINO-2-[1-(DICYCLOHEXYLPHOSPHINO)ETHYL]FERROCENE;JOSIPHOS SL-J003-2;(S)-(+)-1-[(R)-2-(Dicyclohexylphosphino)ferrocenyl]ethyldicyclohexylphosphine

This substance (CAS No.: 158923-07-0), 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 interact with other atoms or molecules through covalent or coordinate bonds to form a stable chemical structure. Its physicochemical properties include specific melting and boiling points, solubility, and chemical stability. These characteristics are closely related to its intramolecular electronic effects, such as the inductive and conjugation effects jointly regulating the distribution of molecular orbital energy levels, forming an extended conjugated system to enhance electron delocalization. The stability of this substance is synergistically influenced by steric hindrance and electronic effects, exhibiting excellent resistance to deactivation in catalytic reactions. Its catalytic activity stems from the selective adsorption and activation of the substrate by the active site, while its coordination properties, through the formation of stable coordinate bonds with the metal center via lone pairs of electrons or π orbitals, regulate the oxidation state and geometry of the metal, thereby affecting the energy barrier and selectivity of the catalytic cycle. In application areas, this substance, as a catalyst, can efficiently promote organic synthesis reactions (such as cross-coupling and asymmetric hydrogenation), significantly improving reaction rates and product yields. Simultaneously, it stabilizes active metal intermediates through coordination, reducing side reactions. As a ligand, its unique electron-donating properties allow for precise modulation of the electronic structure of metal catalysts, optimizing catalytic performance, particularly in homogeneous catalytic systems. Its core applications cover key industrial processes such as pharmaceutical intermediate synthesis, polymer polymerization, and fine chemical preparation, achieving green chemistry goals by reducing energy consumption and waste emissions. In terms of industry value, this substance extends equipment lifespan by improving catalytic efficiency and reduces production costs. Furthermore, its high selectivity and environmental friendliness meet the requirements of modern chemical industry for sustainable development, giving it an irreplaceable strategic position in high-end manufacturing fields such as OLED material synthesis.