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, name: 1,2-Bis(diphenylphosphino)benzene
An ionic chromium(III) species, [CrCl2(THF)4] [Al(OC4F9)4] (2), has been synthesized and is shown to react with a variety of bidentate diphosphine ligands to yield complexes of the type [CrCl2(diphosphine)2][Al(OC 4F9)4]. When compound 2 is combined with diphosphines Ar2PN(Me)PAr2 (Ar = 2-MeO-C6H 4) and Ph2PN(i-Pr)PPh2, after activation with small amounts of AlMe3, active species for the selective oligomerization of ethylene with catalyst productivities of up to 25010 g g Cr-1 h-1 are observed. Selectivity to 1-hexene or 1-octene is a function of ligand structure in an identical fashion to the MAO-activated system. A novel Cr(II) species, [Cr(Ar2PN(Me)PAr 2)2][Al(OC4F9)4] 2 (5), was isolated from the catalytic mixture. Compound 5 alone does not oligomerize ethylene, but reaction with MAO yields a highly active catalyst for selective ethylene oligomerization.
Sometimes chemists are able to propose two or more mechanisms that are consistent with the available data.name: 1,2-Bis(diphenylphosphino)benzene, If a proposed mechanism predicts the wrong experimental rate law, however, the mechanism must be incorrect.Welcome to check out more blogs about 13991-08-7, in my other articles.
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