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A reaction mechanism is the microscopic path by which reactants are transformed into products. Each step is an elementary reaction. In my other articles, you can also check out more blogs about 108-47-4

Related Products of 108-47-4, The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.108-47-4, Name is 2,4-Dimethylpyridine, molecular formula is C7H9N. In a Article£¬once mentioned of 108-47-4

The reactivity of cationic platinum(II) complexes containing the tridentate ligand bis(2-pyridylmethyl)sulphide

The kinetics of the displacement of coordinated nitrogen donor bases (L)by chloride from complexes of the type [Pt(NSN)(L)](2+) [NSN=bis(2-pyri dylmethyl)sulphide; L=a series of pyridines, isoquinoline and NH3] as well as chloride substitution from the substrate [Pt(NSN)Cl](+) by Br(-) and I(-) have been studied in methanol at 25¡ãC and constant ionic strength and compared with those of the corresponding platinum(II) complexes containing the 2,6-bis(methylsulphanyl)pyridine tridentate ligand. The two-term rate law usually found in substitutions at square-planar platinum(II) complexes is obeyed. Both the first and second-order rate constants for the displacement of L decrease as the basicity of the leavinggroup increases. pi interactions between coordinated pyridines and th e metal centre are suggested by comparison of their lability with that of ammonia as well as with that of para-substituted pyridines with enhanced pi system. Steric hindrance on the leaving base also significantly decreases the reactivity.

A reaction mechanism is the microscopic path by which reactants are transformed into products. Each step is an elementary reaction. In my other articles, you can also check out more blogs about 108-47-4

Reference£º
Chiral nitrogen ligands in late transition metal-catalysed asymmetric synthesis¡ªI. Addressing the problem of ligand lability in rhodium-catalysed hydrosilations,
Nitrogen-Containing Ligands for Asymmetric Homogeneous and Heterogeneous Catalysis