The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.92361-49-4, Name is Chloro(pentamethylcyclopentadienyl)bis(triphenylphosphine)ruthenium(II), molecular formula is C46H45ClP2Ru. In a Article，once mentioned of 92361-49-4, Application In Synthesis of Chloro(pentamethylcyclopentadienyl)bis(triphenylphosphine)ruthenium(II)
The bimetallic complexes CpRu(P-P)X [Cp = n5-C5H 5; X = Cl, H; P-P = dppf (1,1?-bis(diphenylphosphino)ferrocene) , dppr (1,1?-bis(diphenylphosphino)ruthenocene), dppo (1,1?- bis(diphenylphosphino)-osmocene), dippf (1,1?-bis(diisopropylphosphino) ferrocene), dcpf (1,1?-bis(dicyclohexylphosphino)ferrocene)], Cp*Ru(P-P)X [Cp* = n5-C5Me5; X = Cl, H; P-P = dppf, dippf, dppomf (1,1?-bis(diphenylphosphino) octamethylferrocene), dppc (1,1?-bis(diphenylphosphino)cobaltocene)], [Cp*Ru(P-P)X]+ (X = H, CCPh; P-P = dppc+), and [Cp*Ru(P-P)L]2+ (L = CH3CN, t-BuCN; P-P = dppc -) have been synthesized. Most of the chloride and hydride complexes have been studied by cyclic voltammetry. The X-ray structures of [Cp*Ru(dppc)CH3CN][PF6]2 and [Cp*Ru(dppc)CCPh] [PF6] have been determined. Protonation of [Cp*Ru(dppc)CCPh] + gives the vinylidene complex [Cp*Ru(dppc)CCHPh]2+. The Co(III/II) potential of the dppc+ ligand undergoes a cathodic shift upon coordination in [Cp*Ru-(dppc)H]+ and an anodic shift upon coordination in [Cp*Ru(dppc)CH3CN] . The 1H NMR spectrum of Cp*Ru(dppc)H is consistent with its formulation as a Co(II)/Ru(II) complex. As gauged by their reactivity toward iminium cations, the hydride complexes are poor hydride donors; proton and electron transfer are dominant. CpRu(dippf)H and CpRu(dcpf)H deprotonate iminium cations with acidic a-hydrogens. Cp*Ru(dppc)H is oxidized by the N-(benzylidene)pyrrolidinium cation, giving [Cp*Ru-(dppc)H]- and the vicinal diamine 1,2-bis(N-pyrrolidino)-1,2-diphenylethane. Most of the hydride complexes give rraw-dihydride cations upon protonation; an exception is [Cp*Ru(dppc)H] +, which forms a dihydrogen complex [Cp*Ru(dppc)(H2)]2+ with surprising kinetic stability. This dihydrogen complex is more acidic and less thermodynamically stable than its dihydride isomer. The H2 ligand in [Cp*Ru(dppc)-(H2)]2+ is readily replaced by nitriles; the reaction with t-BuCN occurs by a dissociative mechanism.
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 92361-49-4 is helpful to your research., COA of Formula: C46H45ClP2Ru
Reference：
Highly efficient and robust molecular ruthenium catalysts for water oxidation,
Catalysts | Special Issue : Ruthenium Catalysts – MDPI