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. 19845-69-3, Name is 1,6-Bis(diphenylphosphino)hexane, molecular formula is C30H32P2. In a Article£¬once mentioned of 19845-69-3, Safety of 1,6-Bis(diphenylphosphino)hexane
CLEAVAGE OF PHOSPHOROUS-CARBON BONDS WITH SODIUM/NAPHTHALENE. FACILE PREPARATION OF UNSYMMETRICAL DIPHOSPHINES
Sodium/naphthalene was found to be a homogeneous, mild and selective reagent for the reductive cleavage of aryl-phosphorous bonds.Such cleavage reactions are very useful in the convenient synthesis of unsymmetrical diphosphines from commercially available and air-stable diphosphines.
Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.Safety of 1,6-Bis(diphenylphosphino)hexane. In my other articles, you can also check out more blogs about 19845-69-3
Reference£º
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