Dichloro(1,10-phenanthroline)copper(II)

Catsyn offer gram to tons of Dichloro(1,10-phenanthroline)copper(II) | CAS 14783-09-6, its formula is C12H8N2.Cl2Cu, molecular weight is 314.661g/mol and the purity is usually 98% Min..

Synonyms : (1,10-PHENANTHROLINE)COPPER(II) DICHLORIDE;DICHLORO(1,10-PHENANTHROLINE)COPPER(II);DICHLORO(1,10-PHENATHROLINE)COPPER(II)

This substance (CAS No.: 14783-09-6), acting as both a catalyst and a ligand, typically possesses specific functional groups or metal binding sites in its molecular structure, endowing it with unique physicochemical properties. Its electronic effects can be modulated by the electron-withdrawing or electron-donating characteristics of substituents, influencing intramolecular charge distribution and reactivity. The energy level structure is determined by molecular orbital theory; the band gap between the highest occupied molecular orbital (HOMO) and the lowest unoccupied molecular orbital (LUMO) directly affects its redox capacity and photoluminescence performance. The expansion of the conjugated system can enhance intramolecular π-electron delocalization, improve stability, and lower the activation energy, thereby optimizing catalytic activity. As a ligand, its spatial configuration and electron-donating ability determine its coordination mode with the metal center, forming a stable metal-ligand complex, which in turn regulates the selectivity and efficiency of the catalytic reaction. This substance exhibits good thermodynamic and kinetic stability, maintaining structural integrity over a wide temperature range. Furthermore, its coordination sites can flexibly adapt to various metal ions, forming a highly efficient catalytic system. In application fields, this substance is widely used as a catalyst and ligand in organic synthesis, homogeneous catalysis, and materials science. Its core function lies in stabilizing the active metal center through coordination, lowering the reaction energy barrier, and improving reaction rate and selectivity, especially in asymmetric catalysis, where it can efficiently synthesize chiral molecules. In the field of OLED materials, as a functional ligand, it can regulate the luminescence performance of metal complexes, optimizing device efficiency and lifetime. Its industry value lies in its ability to replace traditional highly toxic or inefficient catalysts, promoting the development of green chemistry; simultaneously, through molecular design, its catalytic performance can be customized to meet the demands of fine chemicals, pharmaceuticals, and high-end electronic materials for high-purity, highly selective products, significantly reducing production costs and improving process sustainability.