Extracurricular laboratory:new discovery of 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

The aquaorganotin moiety in the title adduct, [SnCl-(C6H5)3(H2O).C 16H16N2, is linked by hydrogen bonds through its axially bonded water molecule to the sub-stituted 1,10-phenanthroline moiety. The Sn atom has trans-trigonal bipyramidal coordination, with aqua and chloro ligands in the axial positions.

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