Electric Literature of 15746-57-3, Catalysts are substances that increase the reaction rate of a chemical reaction without being consumed in the process. 15746-57-3, Name is Cis-Dichlorobis(2,2′-bipyridine)ruthenium(II), molecular formula is C20H16Cl2N4Ru. In a Article，once mentioned of 15746-57-3
A series of three new complexes of the design [(TL)2Ru(BL)]2+, two new complexes of the design [(TL)2Ru(BL)Ru(TL)2]4+, and three new complexes of the design [(TL)2Ru(BL)RhCl2(TL)]3+ (TL = bpy or d8-bpy; BL = dpp or d10-dpp; TL = terminal ligand; BL = bridging ligand; bpy = 2,2?-bipyridine; dpp = 2,3-bis(2-pyridyl)pyrazine) were synthesized and the 1H NMR spectroscopy, electrochemistry, electronic absorbance spectroscopy, and photophysical properties studied. Incorporation of deuterated ligands into the molecular architecture simplifies the 1H NMR spectra, allowing for complete 1H assignment of [(d8-bpy)2Ru(dpp)](PF6)2 and partial assignment of [(bpy)2Ru(d10-dpp)](PF6)2. The electrochemistry for the deuterated and nondeuterated species showed nearly identical redox properties. Electronic absorption spectroscopy of the deuterated and nondeuterated complexes are superimposable with the lowest energy transition being Ru(dpi) ? BL(pi) charge transfer in nature (BL = dpp or d10-dpp). Ligand deuteration impacts the excited-state properties with an observed increase in the quantum yield of emission (Phiem) and excited-state lifetime (tau) of the Ru(dpi) ? d10-dpp(pi) triplet metal-to-ligand charge transfer (3MLCT) excited state when dpp is deuterated, and a decrease in the rate constant for nonradiative decay (knr). Choice of ligand deuteration between bpy and dpp strongly impacts the observed photophysical properties with BL = d10-dpp complexes showing an enhanced Phiem and tau, providing further support that the lowest electronic excited state populated via UV or visible excitation is the photoactive Ru(dpi) ? dpp(pi) CT excited state. The Ru(II),Rh(III) complex incorporating the deuterated BL shows increased hydrogen production compared to the variants incorporating the protiated BL, while demonstrating identical dynamic quenching behaviors in the presence of sacrificial electron donor. (Graph Presented).
The proportionality constant is the rate constant for the particular unimolecular reaction. the reaction rate is directly proportional to the concentration of the reactant. I hope my blog about 15746-57-3 is helpful to your research., Electric Literature of 15746-57-3
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Highly efficient and robust molecular ruthenium catalysts for water oxidation,
Catalysts | Special Issue : Ruthenium Catalysts – MDPI