(1R,2R)-(-)-1,2-Cyclohexanediamino-N,N'-bis(3,5-di-t-butylsalicylidene)cobalt(II)

Catsyn offer gram to tons of (1R,2R)-(-)-1,2-Cyclohexanediamino-N,N'-bis(3,5-di-t-butylsalicylidene)cobalt(II) | CAS 176763-62-5, its formula is C36H52CoN2O2, molecular weight is 603.752g/mol and the purity is usually 98% Min..

Synonyms : (1R,2R)-(-)-1,2-CYCLOHEXANEDIAMINO-N,N'-BIS(3,5-DI-T-BUTYLSALICYLIDENE)COBALT(II);(1R,2R)-(-)-N,N'-BIS(3,5-DI-TERT-BUTYLSALICYLIDENE)-1,2-CYCLOHEXANEDIAMINOCOBALT(II);(R,R)-(-)-N,N'-BIS(3,5-DI-TERT-BUTYLSALICYLIDENE)-1,2-CYCLOHEXANEDIAMINE-COBALT;(R,R)-(-)-N,N'-BIS(3,5-DI-TERT-BUTYLSALICYLIDENE)-1,2-CYCLOHEXANEDIAMINOCOBALT(II);(R,R)-JACOBSEN'S CATALYST COBALT(II) COMPLEX;(R,R)-JACOBSEN'S COBALT(II) CATALYST

This substance (CAS No.: 176763-62-5), used as a catalyst and ligand, typically contains specific coordinating atoms (such as nitrogen, oxygen, and phosphorus) and a conjugated system in its molecular structure. These structural features endow it with unique physicochemical properties. Its electronic effects can be modulated by the electron-withdrawing or electron-donating properties of substituents, thereby affecting the distribution of molecular orbital energy levels, especially the band gap between the highest occupied molecular orbital (HOMO) and the lowest unoccupied molecular orbital (LUMO), which is crucial for electron transfer processes in catalytic reactions. The expansion of the conjugated system can enhance intramolecular π-electron delocalization, improve stability, and lower the activation energy of the reaction, thus optimizing catalytic activity. As a ligand, its steric hindrance and electron-donating ability directly affect the coordination environment of the metal center, thereby regulating the geometry and redox properties of the metal-ligand complex, ultimately determining catalytic selectivity and efficiency. This substance exhibits good thermodynamic stability, maintaining structural integrity over a wide temperature range. Its chemical stability also allows it to remain active in various reaction media, making it suitable for both homogeneous and heterogeneous catalytic systems. In application fields, this substance serves extensively as a catalyst and ligand in core industries such as organic synthesis, pharmaceutical intermediate preparation, and OLED material development. In organic catalysis, it forms active intermediates through coordination with metal centers, efficiently catalyzing key reactions such as carbon-carbon bond formation and asymmetric hydrogenation, significantly improving product yield and enantioselectivity, and reducing industrial synthesis costs. In medicinal chemistry, as a chiral ligand, it can induce stereoselectivity in metal catalysts, facilitating the total synthesis of complex natural products. In the OLED field, this substance participates in the design of phosphorescent materials as a functional ligand, optimizing device luminous efficiency and lifetime by regulating the electronic structure of the metal center, thus driving the upgrade of flexible display and solid-state lighting technologies. Its industry value lies in its role in promoting green chemistry processes, improving atom economy and reducing by-product generation, aligning with the needs of sustainable development, and demonstrating irreplaceable value in the synthesis of high-value-added chemicals, becoming a key bridge connecting basic research and industrialization.