More research is needed about 14220-64-5

Application of 14220-64-5, 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. 14220-64-5, Name is Bis(benzonitrile)palladium chloride, molecular formula is C14H10Cl2N2Pd. In a Article，once mentioned of 14220-64-5

Cationic complexes with a series of tridentate ligands, L = 4X-substituted 2,6-bis(benzimidazol-2-yl)pyridines, 2 (M = Fe or Ni; X = H, OH or Cl), were isolated and characterized, together with the free pyridines, by elemental analysis, Fourier-transform IR, 1H NMR and UV/VIS spectroscopy.The syntheses were performed via condensation of o-phenylenediamine with 4-substituted pyridine-2,6-dicarboxylic acids.Ligand-field parameters were estimated for the nickel complexes.The (2+) species show thermally induced spin-crossover behaviour (1A1 –> 5T2g) which has been investigated in methanol, nitromethane and 20percent (v/v) dimethylformamide in MeOH.The behaviour is complicated by two complex dissociation equilibria, for which equilibrium constants have been evaluated.Ligand substitution is reflected in a change of the spin state in solution (2+) when plotted against Deltadelta (= 1H NMR para increment for substitutions X in benzene) show a turning point in the region around X = H and in this region spin-crossover behaviour is observed.Outside this region there is very little or no such behaviour and it is therefore possible to predict the spin-crossover behaviour for other substituents X from the Deltadelta value.

Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.Application of 14220-64-5. In my other articles, you can also check out more blogs about 14220-64-5

Reference：
Chapter 1 An introduction to palladium catalysis,
Palladium/carbon catalyst regeneration and mechanical application method