The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.32993-05-8, Name is Chlorocyclopentadienylbis(triphenylphosphine)ruthenium(II), molecular formula is C41H35ClP2Ru. In a Article，once mentioned of 32993-05-8, Application In Synthesis of Chlorocyclopentadienylbis(triphenylphosphine)ruthenium(II)
The complexes Ru(eta-RC5H4)Cl(PPh3)2 (R = H, CH3, CH3CO) have been shown to react with the anionic S-S donor ligands M1S2CX, (M1 = Na, K, NH4+; X = OR’, NR”2, CN) to give cyclopentadienyl dithiolate complexes of ruthenium(II).Analogous compounds have been obtained from thallium cyclopentadienide and Ru(S2CX)2(PPh3)2.Ru(eta-CH3COC5H4)Cl(PPh3)2 (III) has been made by reaction between acetylcyclopentadiene, RuCl3(aq.), and PPh3 in absolute ethanol.Complexes of formula Ru(eta-RC5H4)(S2CX)(PPh3)2, with the dithiolate ligand monodentate, are obtained when R = H, X = OC6H11; R = CH3, X = OCH3; R = H, CH3, X = CN.In the other cases studied the isolated complexes contain a bidentate S-S ligand.Steric effects as well as the electronic properties of dithiolate ligands, seem to influence the choice between the two coordination modes.Reaction of III with NaS2CNEt2 affords Ru(S2CNEt2)2(PPh3)2 as the sole product.Carbonylation of complex VI, Ru(eta-C5H5)(S2COC6H11)(PPh3)2 takes place in solution, but the carbonyl complex could not be isolated.
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 32993-05-8 is helpful to your research., Application In Synthesis of Chlorocyclopentadienylbis(triphenylphosphine)ruthenium(II)
Reference：
Highly efficient and robust molecular ruthenium catalysts for water oxidation,
Catalysts | Special Issue : Ruthenium Catalysts – MDPI