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

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

  • Catalogue Number : SC11421
  • CAS Number : 167416-28-6
  • MDL Number : MFCD01074441
  • Molecular Formula : C31H51P2.C5H5.Fe
  • Molecular Weight : 606.631
  • Purity : 98% Min.
  • Category : Catalysts and Ligands
Description

Catsyn offer gram to tons of (R)-(-)-1-[(S)-2-(Dicyclohexylphosphino)ferrocenyl]ethyldicyclohexylphosphine | CAS 167416-28-6, its formula is C31H51P2.C5H5.Fe, molecular weight is 606.631g/mol and the purity is usually 98% Min..

Synonyms : (R)-(-)-1-[(S)-2-(DICYCLOHEXYLPHOSPHINO)FERROCENYL]ETHYLDICYCLOHEXYLPHOSPHINE;(R)-1-[(1S)-2-(DICYCLOHEXYLPHOSPHINO)FERROCENYL]ETHYLDICYCLOHEXYLPHOSPHINE;(R)-1-[(SP)-2-(DICYCLOHEXYLPHOSPHINO)FERROCENYL]ETHYLDICYCLOHEXYLPHOSPHINE;JOSIPHOS SL-J003-1

This substance (CAS No.: 167416-28-6), 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 may involve the distribution of electron-donating or electron-withdrawing groups, influencing the energy difference between molecular orbital levels and frontier orbitals (HOMO-LUMO), thereby modulating reaction activity. 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 reaction energy barrier. Its stability may stem from steric hindrance or the formation of strong coordination bonds, while catalytic activity is closely related to the electronic state of the metal center, the coordination environment, and the substrate adsorption capacity. As a ligand, it can coordinate with the metal center in monodentate, bidentate, or multidentate modes to form stable complexes, and optimize catalytic performance by modulating the redox potential or spatial configuration of the metal. This substance has wide applications in materials science and chemical engineering, especially in catalytic reactions where it can significantly improve reaction efficiency and selectivity as a key component. For example, in organic synthesis, it can serve as a homogeneous catalyst to promote carbon-carbon bond formation or asymmetric catalytic reactions; in OLED manufacturing, its coordination properties can be used to modulate the luminescence properties of metal complexes, optimizing device efficiency and lifetime. As a functional ligand, its core applications include stabilizing active metal centers, regulating reaction pathways, and suppressing side reactions, thereby reducing energy consumption and improving product purity. In terms of industry value, this substance promotes technological innovation in green chemistry and high-end manufacturing by enhancing the sustainability and economy of catalytic systems, demonstrating irreplaceable strategic significance, especially in the synthesis of fine chemicals and novel display technologies.

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