Note that a catalyst decreases the activation energy for both the forward and the reverse reactions and hence accelerates both the forward and the reverse reactions.Recommanded Product: 13991-08-7, you can also check out more blogs about13991-08-7
The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.13991-08-7, Name is 1,2-Bis(diphenylphosphino)benzene, molecular formula is C30H24P2. In a Article，once mentioned of 13991-08-7, Recommanded Product: 13991-08-7
The cobalt(I) carbonyl complexes Y, Y2, and Y (L-L = ditertiary phosphine; Y = BF4, BPh4) have been obtained by treating alcoholic solutions of cobalt(II) salts containing weakly-coordinating anions and diphosphines with carbon monoxide under ambient conditions.The types of products formed depend on the steric properties of the ligand L-L.The stereochemistry and dynamic behaviour of the products in solution have been studied by variable-temperature 31P<1H> NMR spectroscopy.A possible mechanism is suggested for the carbonylation reactions, which were found to involve formation of the diphosphine oxides.
Note that a catalyst decreases the activation energy for both the forward and the reverse reactions and hence accelerates both the forward and the reverse reactions.Recommanded Product: 13991-08-7, you can also check out more blogs about13991-08-7
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