The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.12150-46-8, Name is 1,1-Bis(diphenylphosphino)ferrocene, molecular formula is C34H28FeP2. In a Article，once mentioned of 12150-46-8, Product Details of 12150-46-8
A range of ruthenium-arene compounds with chloride, bromide or iodide ligands were prepared and tested as catalysts for the homogeneous redox neutral alkylation of tert-butylamine with phenethyl alcohol, and compared to the previously reported catalyst [RuCl2(p-cymene)]2, in the presence of the diphosphine 1,1?-bis(diphenylphosphino)ferrocene (dppf). The best catalytic activities were obtained with ruthenium iodide compounds. The formation of either [RuX(p-cymene)(dppf)][X] or [(RuX2(p-cymene))2(dppf)] (X = halide) under the catalytic conditions employed was investigated. Haloruthenium arene complexes have been tested as catalysts for the homogeneous redox neutral alkylation of tert-butylamine with phenethyl alcohol in the presence of 1,1?-bis(diphenylphosphino)ferrocene (dppf). Halide identity and arene substitutions influence the catalytic activity and both RuX(p-cymene)(dppf)][X] and [(RuX2(p-cymene))2(dppf)] (X = halide) appear to play a role in catalysis.
The reactant in an enzyme-catalyzed reaction is called a substrate. Enzyme inhibitors cause a decrease in the reaction rate of an enzyme-catalyzed reaction.I hope my blog about 12150-46-8 is helpful to your research., Product Details of 12150-46-8
Reference：
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