Copper(II) hexafluoroacetylacetonate, anhydrous,  Cu(CF3COCHCOCF3)2

Catsyn offer gram to tons of Copper(II) hexafluoroacetylacetonate, anhydrous,  Cu(CF3COCHCOCF3)2 | CAS 14781-45-4, its formula is C10H2CuF12O4, molecular weight is 477.644g/mol and the purity is usually 98% Min..

Synonyms : BIS(HEXAFLUOROACETYLACETONATO) COPPER(II);COPPER HEXAFLUOROACETYLACETONATE;COPPER(2+) ION BIS((2Z)-1,1,1,5,5,5-HEXAFLUORO-4-OXOPENT-2-EN-2-OLATE);COPPER(II) HEXAFLUORO-2,4-PENTANEDIONATE;COPPER(II) HEXAFLUOROACETYLACETONATE;Copper(II) hexafluoroacetylacetonate, anhydrous,? Cu(CF3COCHCOCF3)2

This substance (CAS No.: 14781-45-4), 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 stable chemical structures. 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 inductive and conjugation effects jointly regulating the distribution of molecular orbital energy levels, forming delocalized π bonds or σ-π hyperconjugated systems, thereby enhancing molecular stability. As a catalyst, its active center promotes electron transfer or bond recombination processes by lowering the reaction activation energy, exhibiting high selectivity and efficiency. As a ligand, its lone pair electrons or π electron cloud can form stable coordinate bonds with the metal center, regulating the redox properties and geometry of the metal center through steric hindrance and electronic effects, thus affecting the rate of the catalytic cycle and product distribution. This substance has wide applications in organic synthesis, homogeneous catalysis, and materials science. Its core function lies in regulating chemical reaction pathways through coordination or catalytic active centers. In organic synthesis, it can act as a chiral ligand to form complexes with transition metals, enabling high-value-added reactions such as asymmetric catalytic hydrogenation and cyclopropanation, significantly improving product enantioselectivity. In homogeneous catalysis, its unique electronic structure can optimize the electronic state of metal centers, enhancing the catalyst's adsorption and activation capabilities for substrates, making it suitable for key industrial reactions such as olefin polymerization and cross-coupling. Furthermore, in OLED material fabrication, this substance serves as a dopant or functional layer component, improving device luminous efficiency and stability by regulating carrier mobility and energy level matching, demonstrating interdisciplinary industry value, and holding an irreplaceable strategic position, particularly in fine chemicals, new energy, and display technology.