Di-μ-chlorobis[2-[(dimethylamino)methyl]phenyl-C,N]dipalladium(II)

Catsyn offer gram to tons of Di-μ-chlorobis[2-[(dimethylamino)methyl]phenyl-C,N]dipalladium(II) | CAS 18987-59-2, its formula is 2C9H12ClNPd, molecular weight is 552.148g/mol and the purity is usually 98% Min..

Synonyms : DI-MU-CHLORO-BIS[2-(DIMETHYLAMINOMETHYL)PHENYL-C(1),N]DIPALLADIUM(II);DI-MU-CHLOROBIS[2-[(DIMETHYLAMINO)METHYL]PHENYL-C,N]DIPALLADIUM(II);DI-MU-CHLOROBIS[2-[(DIMETHYLAMINO)METHYL]PHENYL]DIPALLADIUM;Di-μ-chlorobis[2-[(dimethylamino)methyl]phenyl-C,N]dipalladium(II)

This substance (CAS No.: 18987-59-2), used as a catalyst and ligand, typically contains heteroatoms (such as nitrogen, oxygen, and phosphorus) or π-conjugated systems with lone pairs of electrons in its molecular structure, enabling it to form stable complexes with the metal center through coordinate bonds. Its physicochemical properties include moderate solubility in common solvents, melting and boiling points depending on the strength of intermolecular forces, and low surface tension that facilitates sufficient contact with reactants. In terms of electronic effects, the ligand modulates the electron density of the metal center through electron-donating or electron-withdrawing groups, thereby affecting the redox potential of the catalytically active center. The energy level distribution shows a moderate gap between its highest occupied molecular orbital (HOMO) and lowest unoccupied molecular orbital (LUMO), which is beneficial for electron transfer processes. The presence of the conjugated system enhances the intramolecular electron delocalization ability and improves coordination stability, exhibiting excellent resistance to hydrolysis and oxidation, especially in transition metal catalytic systems. Its catalytic activity stems from its stabilizing effect on reaction intermediates, synergistically regulating reaction pathway selectivity through steric hindrance and electronic effects. Its coordination properties exhibit high affinity for various metal ions (such as Pd, Ru, and Ir), forming monodentate, bidentate, or multidentate complexes, significantly improving the turnover rate of metal catalysts and product yield. In application fields, this substance is widely used as a key catalyst and ligand in organic synthesis, pharmaceutical intermediate preparation, and OLED material manufacturing. Its function lies in reducing the reaction activation energy through a coordination-activation mechanism, achieving efficient construction of carbon-carbon and carbon-heteroatom bonds, especially demonstrating excellent chiral induction ability in asymmetric catalysis. Core applications include cross-coupling processes such as Suzuki coupling and Heck reactions, as well as redox reactions such as hydrogenation and oxidation, significantly improving reaction selectivity and atom economy. In the OLED industry, as a ligand for phosphorescent complexes, it optimizes device luminous efficiency and color purity by regulating the triplet energy level of the metal center, promoting the commercialization of flexible displays and solid-state lighting technologies. Its industry value lies in its high activity and stability, which can reduce catalyst usage and lower production costs. Furthermore, its designability provides a structural basis for developing novel catalytic systems, holding significant strategic importance for green chemistry and high-end materials manufacturing.