More research is needed about 3,4,7,8-Tetramethyl-1,10-phenanthroline

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.Application of 1660-93-1, you can also check out more blogs about1660-93-1

Application of 1660-93-1, 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. 1660-93-1, Name is 3,4,7,8-Tetramethyl-1,10-phenanthroline, molecular formula is C16H16N2. In a Article，once mentioned of 1660-93-1

In the presence of an iridium 3,4,7,8-tetramethyl-1,10-phenanthroline catalyst, a methyl group on the silicon atom of alkyltrimethylsilanes undergoes selective C-H borylation with bis(pinacolato)diboron in cyclooctane at 135 C to give alkyl(borylmethyl)dimethylsilanes. The C-H borylation of tetramethylsilane takes place efficiently at 100 C. Permethyloligosilanes can also undergo C-H borylation without cleavage of the Si-Si bonds.

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.Application of 1660-93-1, you can also check out more blogs about1660-93-1

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