Reference of 1762-46-5, 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. 1762-46-5, Name is Diethyl [2,2′-bipyridine]-5,5′-dicarboxylate, molecular formula is C16H16N2O4. In a Article，once mentioned of 1762-46-5
The electronic absorption and resonance Raman spectra of the reduction products of some tris(5,5′-substituted bipyridine) complexes of iron and osmium provide “model” behavior for single-ligand localized redox orbitals.While the electron-withdrawing nature of the ethylcarboxy and phenyl substituents allows for the stable electrochemical addition of six electrons, the physical measurements are explicable within the framework developed for the tris bipyridine compounds, for which only the first three reduction products have been studied.Therefore, addition of more than one electron per ligand does not disrupt the localization mechanism for this set of iron and osmium complexes.Furthermore, the effects of ? back-bonding to these ligands are explored by comparing the results for the different metals.
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.Reference of 1762-46-5, you can also check out more blogs about1762-46-5
Reference：
Metal catalyst and ligand design,
Ligand Template Strategies for Catalyst Encapsulation – NCBI