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. 246047-72-3, Name is (1,3-Bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene)dichloro(phenylmethylene)(tricyclohexylphosphine)ruthenium, molecular formula is C46H65Cl2N2PRu. In a Article，once mentioned of 246047-72-3, Recommanded Product: (1,3-Bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene)dichloro(phenylmethylene)(tricyclohexylphosphine)ruthenium
The activity and stereoselectivity of phosphane- and N-heterocyclic carbene (NHC)-containing ruthenium benzylidene complexes have been evaluated in macrocyclic ring-closing olefin metathesis to produce unsaturated lactones and lactams. The success of the macrocyclization depends on the nature of the ligand (phosphane or N-heterocyclic carbene) on the ruthenium center and on the NHC properties. As for stereoselectivity, E/Z ratios seem to be influenced not only by the nature of the ruthenium catalyst but also by the thermodynamic stabilities of the resulting unsaturated macrocycles, as confirmed by theoretical results. The synthesis of 14-and 15-membered macrolactones and macrolactams by ruthenium-catalyzed ring-closing metathesis is investigated. The reaction outcome is influenced both by the nature of the catalyst and the diene substrate.
Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.Application In Synthesis of (1,3-Bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene)dichloro(phenylmethylene)(tricyclohexylphosphine)ruthenium. In my other articles, you can also check out more blogs about 246047-72-3
Reference：
Highly efficient and robust molecular ruthenium catalysts for water oxidation,
Catalysts | Special Issue : Ruthenium Catalysts – MDPI