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Note that a catalyst decreases the activation energy for both the forward and the reverse reactions and hence accelerates both the forward and the reverse reactions.category: ruthenium-catalysts, you can also check out more blogs about32993-05-8

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, category: ruthenium-catalysts

Hexa- and nonanitrile ligands were synthesized by the known CpFe +-induced hexaallylation of hexamethylbenzene in [FeCp(n 6-C6Me6)] [PF6] and nonaallylation of mesitylene in [FeCp(n6-l,3,5-C6H3Me 3],[PF6], respectively, followed by Pt-catalyzed regioselective hydrosilylation of the iron-free polyolefins using (chloromethyl)dimethylsilane and sodium iodide catalyzed Williamson coupling with p-hydroxybenzonitrile. The hexanitrile star was coordinated to the piano-stool ruthenium complex [RuCp(PPh3)2Cl] by substitution of the six ruthenium-bound chlorides with nitriles using TIPF 6 to give the hexacationic hexaruthenium star complex, whereas the analogous metalation reaction partly failed, due to bulk constraint with the nonanitrile ligand. The strategy that involved lengthening of the tethers of the latter, however, successfully provided a nonacationic nonaruthenium complex.

Note that a catalyst decreases the activation energy for both the forward and the reverse reactions and hence accelerates both the forward and the reverse reactions.category: ruthenium-catalysts, you can also check out more blogs about32993-05-8

Reference:
Highly efficient and robust molecular ruthenium catalysts for water oxidation,
Catalysts | Special Issue : Ruthenium Catalysts – MDPI