Bis{2-[(11bR)-3,5-dihydro-4H-dinaphtho[2,1-c:1',2'-e]phosphepin-4-yl]ethyl}amine

Catsyn offer gram to tons of Bis{2-[(11bR)-3,5-dihydro-4H-dinaphtho[2,1-c:1',2'-e]phosphepin-4-yl]ethyl}amine | CAS 851870-89-8, its formula is C48H41NP2, molecular weight is 693.807g/mol and the purity is usually 98% Min..

Synonyms : 2,2'-BIS[(R-1,1'-BINAPHTHYL-2,2'-DIMETHYL)PHOSPHINO]DIETHYLAMINE;2,2'-BIS[(S-1,1'-BINAPHTHYL-2,2'-DIMETHYL)PHOSPHINO]DIETHYLAMINE;BIS(R-2-(4,5-DIHYDRO-3H-BINAPHTHO[1,2-C:2',1'-E]-PHOSPHEPINO)ETHYL)AMINE;BIS(S-2-(4,5-DIHYDRO-3H-BINAPHTHO[1,2-C:2',1'-E]-PHOSPHEPINO)ETHYL)AMINE;BIS[2-[(11BR)-3,5-DIHYDRO-4H-DINAPHTHO[2,1-C:1',2'-E]PHOSPHEPIN-4-YL]ETHYL]AMINE;BIS[2-[(11BS)-3,5-DIHYDRO-4H-DINAPHTHO[2,1-C:1',2'-E]PHOSPHEPIN-4-YL]ETHYL]AMINE;Bis{2-[(11bR)-3,5-dihydro-4H-dinaphtho[2,1-c:1',2'-e]phosphepin-4-yl]ethyl}amine

Substance 851870-89-8, used as a catalyst and ligand, typically contains specific functional groups and conjugated systems in its molecular structure, which endow it with unique physicochemical properties. This substance may possess a suitable molecular weight and good solubility, enabling it to exist stably in specific solvents. Its electronic effects regulate the intramolecular charge distribution through the electron-withdrawing or electron-donating properties of substituents, thereby affecting the energy level structure and reaction activity. The expansion of the conjugated system enhances the overlap of molecular orbitals, improves electron delocalization, and helps stabilize intermediates or transition states, thus enhancing catalytic activity. Regarding coordination properties, this substance may contain polydentate coordinating groups, capable of forming stable coordination bonds with the metal center. It regulates the electronic state and geometry of the metal center through steric hindrance and electronic effects, thereby optimizing catalytic performance. Its stability is supported by intramolecular hydrogen bonds, π-π stacking, and other non-covalent interactions, ensuring structural integrity during catalytic reactions. In application fields, substance 851870-89-8, as a catalyst or ligand, is widely used in organic synthesis, asymmetric catalysis, and materials science. Its core function lies in achieving efficient and green chemical transformations by regulating reaction pathways, lowering activation energies, or improving selectivity. For example, in asymmetric catalysis, this substance can act as a chiral ligand to induce stereoselectivity in metal catalysts, synthesizing high-value-added chiral molecules; in materials science, its coordination properties can be used to construct metal-organic frameworks (MOFs) or coordination polymers, regulating the photoelectric properties and catalytic activity of materials. Its industry value lies in its ability to significantly improve reaction efficiency and product purity, reduce byproduct formation, lower production costs, and simultaneously promote the advancement of green chemistry and sustainable development technologies, holding irreplaceable strategic significance, especially in pharmaceuticals, fine chemicals, and OLED display materials.