A catalyst don’t appear in the overall stoichiometry of the reaction it catalyzes, but it must appear in at least one of the elementary reactions in the mechanism for the catalyzed reaction. 224311-51-7, Name is 2-(Di-tert-Butylphosphino)biphenyl, molecular formula is C20H27P. In a Article£¬once mentioned of 224311-51-7, Product Details of 224311-51-7
Rhodium-Catalyzed ortho-Selective C-F Activation and Hydrodefluorination of Heterocycle-Substituted Polyfluoroarenes: Dominated by Phosphine Ligands
In this paper, the ortho-selective mono-hydrodefluorination and/or di-hydrodefluorination of heterocycle substituted polyfluoroarenes were catalyzed by rhodium complexes along with phosphine ligands and ethanol as hydride source. Diverse partially fluorinated aromatics had been synthesized by this method. The study of the mechanism demonstrated that ethanol was the sole hydride source in the cycle of hydrodefluorination. Furthermore, the phosphine ligand controlled chemoselectivity had been discussed by monitoring experiment.
Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.Product Details of 224311-51-7. In my other articles, you can also check out more blogs about 224311-51-7
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Phosphine ligand,
Chiral phosphine ligands in asymmetric synthesis. Molecular structure and absolute configuration of (1,5-cyclooctadiene)-(2S,3S)-2,3-bis(diphenylphosphino)butanerhodium(I) perchlorate tetrahydrofuran solvate