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Tetrakis[N-phthaloyl-(R)-tert-leucinato]dirhodium Bis(ethyl Acetate) Adduct

Tetrakis[N-phthaloyl-(R)-tert-leucinato]dirhodium Bis(ethyl Acetate) Adduct

  • Catalogue Number : SC10376
  • CAS Number : 380375-05-3
  • MDL Number : MFCD06797189
  • Molecular Formula : C56H56N4O16Rh2.2C4H8O2
  • Molecular Weight : 1423.1
  • Purity : 98% Min.
  • Category : Catalysts and Ligands
Description

Catsyn offer gram to tons of Tetrakis[N-phthaloyl-(R)-tert-leucinato]dirhodium Bis(ethyl Acetate) Adduct | CAS 380375-05-3, its formula is C56H56N4O16Rh2.2C4H8O2, molecular weight is 1423.1g/mol and the purity is usually 98% Min..

Synonyms : DIRHODIUM TETRAKIS[N-PHTHALOYL-(R)-TERT-LEUCINATE] BIS(ETHYL ACETATE) ADDUCT;TETRAKIS[N-PHTHALOYL-(R)-TERT-LEUCINATO]DIRHODIUM BIS(ETHYL ACETATE) ADDUCT

This substance (CAS No.: 380375-05-3), acting as a catalyst and ligand, typically contains specific functional groups or heteroatoms (such as nitrogen, oxygen, and phosphorus) in its molecular structure. These groups are linked to other atoms or groups through covalent or coordinate bonds, forming molecules with specific spatial configurations. Its physicochemical properties include specific melting and boiling points, solubility, and chemical stability. These properties are significantly influenced by intramolecular electronic effects (such as inductive and conjugation effects). These electronic effects further regulate the molecular energy level distribution, especially the energy difference between the highest occupied molecular orbital (HOMO) and the lowest unoccupied molecular orbital (LUMO), thus affecting its photochemical and electrochemical properties. Conjugated systems within the molecule (such as π-π conjugation or p-π conjugation) can enhance intramolecular electron delocalization, improve stability, and lower the activation energy, resulting in high activity in catalytic reactions. As a ligand, its lone pair electrons or π electrons can form stable coordinate bonds with the metal center, modulating the catalytic performance of the metal center, such as selectivity, conversion rate, and reaction rate, through steric hindrance and electron-donating ability. This substance has wide applications in materials science, organic synthesis, and OLEDs. As a catalyst, its core function is to lower reaction energy barriers, accelerate specific chemical reactions (such as oxidation, reduction, and coupling reactions), and achieve high-yield synthesis of target products through selective regulation, making it valuable in the preparation of pharmaceutical intermediates, fine chemicals, and polymer materials. As a ligand, its complexes with metals can be applied to homogeneous catalytic systems, significantly improving catalytic efficiency and selectivity, especially in asymmetric catalysis, providing an efficient pathway for the synthesis of chiral compounds. In the OLED field, this substance or its derivatives can serve as functional materials, optimizing device luminous efficiency and stability by regulating molecular energy levels and carrier transport performance, thus driving the iterative upgrade of display technology. Its industry value lies in improving production efficiency, reducing energy consumption, and promoting green chemistry, serving as a key bridge connecting basic research and industrial applications.

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