Can You Really Do Chemisty Experiments About 2,4,6-Triphenylpyrylium tetrafluoroborate

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.Synthetic Route of 448-61-3, you can also check out more blogs about448-61-3

Synthetic Route of 448-61-3, 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. 448-61-3, Name is 2,4,6-Triphenylpyrylium tetrafluoroborate, molecular formula is C23H17BF4O. In a Article，once mentioned of 448-61-3

The quarternary pyridinium salts Ia-Ic react with alkaline solution of potassium ferricyanide to give the condensed heterocyclic derivatives IIIa,b,IV,whereas the salts Id-If give the pyrrole derivatives IIa-IIc under the same conditions.The diaza heterocycle IIIa reacts with methyl iodide to give methoiodide V,whereas by action of bromine it produces two monobromo derivatives VIa,b.The pyrrole derivatives IIa,b give monobromo derivatives IId,e on bromination.A probable mechanism of formation of the heterocyclic derivatives is discussed.

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.Synthetic Route of 448-61-3, you can also check out more blogs about448-61-3

Reference：
Metal catalyst and ligand design,
Ligand Template Strategies for Catalyst Encapsulation – NCBI