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![(S)-(-)-[(S)-2-Diphenylphosphinoferrocenyl][2-bis(3,5-dimethyl-4-methoxyphenyl)phosphinophenyl]methanol](https://qncdn.chemcd.cn/catsyn/structure/SC11439.png)
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Catsyn offer gram to tons of (S)-(-)-[(S)-2-Diphenylphosphinoferrocenyl][2-bis(3,5-dimethyl-4-methoxyphenyl)phosphinophenyl]methanol | CAS 851308-47-9, its formula is C42H41O3P2.C5H5.Fe, molecular weight is 776.67g/mol and the purity is usually 98% Min..
Synonyms : (S)-(-)-[(S)-2-DIPHENYLPHOSPHINOFERROCENYL][2-BIS(3,5-DIMETHYL-4-METHOXYPHENYL)PHOSPHINOPHENYL]METHANOL
851308-47-9, as an organic compound with a specific structure, contains multiple functional groups in its molecular structure. These groups are connected by covalent bonds to form a specific spatial configuration, endowing it with unique physicochemical properties. This substance has a moderate molecular weight and good solubility, and can exist stably in a variety of organic solvents. Its electronic effects are reflected in the distribution of the intramolecular electron cloud, influencing the reactivity of the molecule through inductive and conjugation effects. The formation of the conjugated system significantly lowers the molecular energy level and enhances its electron transfer ability. In terms of stability, this compound exhibits good thermal and chemical stability, maintaining structural integrity over a wide temperature and pH range. As a catalyst, its catalytic activity stems from the coordination ability and electron transfer ability of specific groups in the molecule, effectively reducing the activation energy of the reaction and promoting the target reaction. Simultaneously, as a ligand, its multidentate coordination structure can form stable complexes with metal ions, and the properties and reactivity of the complexes are modulated through steric hindrance and electronic effects.
851308-47-9 shows broad application value in materials science, organic synthesis, and OLED fields.
As a catalyst, it can efficiently catalyze a variety of organic reactions, such as cross-coupling reactions and redox reactions, significantly improving reaction yield and selectivity while reducing production costs. In ligand applications, its complexes with metal ions exhibit excellent performance in catalysis, photoluminescence, and electroluminescence, especially as a functional material in OLED devices, optimizing device luminescence performance and stability, and improving display effects and lifespan. Furthermore, as a chiral ligand in asymmetric catalytic synthesis, it enables highly enantioselective synthesis, providing an important means for the preparation of chiral drugs and fine chemicals. Its industry value lies in driving technological progress and industrial upgrading in related fields, meeting the development needs of high-end manufacturing and green chemistry.