The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.50777-76-9, Name is 2-(Diphenylphosphino)benzaldehyde, molecular formula is C19H15OP. In a Article，once mentioned of 50777-76-9, name: 2-(Diphenylphosphino)benzaldehyde
Hydroxyalkyl complexes and hemiaminal formation in the reaction of o-diphenylphosphinobenzaldehyde with rhodium(I) dihydrazone complexes
The diimino complex Rh(COD)(bdh)Cl (bdh: H2NNqqC(Me)C(Me)qqNNH2) reacts with o-diphenylphosphino(benzaldehyde) (PCHO) in the presence of PPh3 to give acylhydrido [Rh(H)(PCO)(PPh3)(bdh)]+ species. When using Rh/PCHO = 1:2 stoichiometric ratios, oxidative addition of one PCHO and P-coordination of another PCHO occurs. The aldehyde group then undergoes two competitive reactions: (i) addition of one free amino group to give a stable hemiaminal and a complex [Rh(H)(PCO)(Pbdh)]+ that contains a new PNN ligand coordinated via the imino nitrogens and the phosphorus atom or (ii) insertion into Rh-H to give the hydroxyalkyl complex [Rh(PCO)(PCHOH)(bdh)]+. The complexes have been fully characterized, and X-ray diffraction structures of both of them are reported. Some intermediates in the competitive reactions have been spectroscopically characterized, and the transformation of the hemiaminal group into imine to give a PaNN ligand in the complex [Rh(H)(PCO)(Pabdh)]+ has also been studied.
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 50777-76-9 is helpful to your research., name: 2-(Diphenylphosphino)benzaldehyde
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