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. 13991-08-7, Name is 1,2-Bis(diphenylphosphino)benzene, molecular formula is C30H24P2. In a Article，once mentioned of 13991-08-7, Product Details of 13991-08-7
Heterobifunctional phosphorus compounds have been prepared by oxidizing one phosphorus atom of a bis(phosphine) with azides.A variety of backbone structures have been used with one and two carbon chains, saturated and unsaturated structures and RN.Some degree of steric control appears to limit the extent of oxidation in cis bis(phosphines) with rigid backbones.Trimethylsilyl azide gives silylated iminophosphoranes with a reactive functionality on the imine nitrogen which can be replaced via metathetical elimination of Me3SiX or converted to the trimethylsilyloxy metal derivative by rearrangement of the trimethylsilyl group to terminal oxygen of a highly oxidized metal oxo precursor.Structural features of several examples of the heterobifunctional phosphorus compounds and their derivatives are described.
Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.Product Details of 13991-08-7. In my other articles, you can also check out more blogs about 13991-08-7
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