Synthetic Route 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
Two mononuclear single molecule magnets derived from dysprosium(iii) and tmphen (tmphen = 3,4,7,8-tetramethyl-1,10-phenanthroline)
Two mononuclear Dy(iii) complexes, [DyIII(hfac)3(tmphen)] (1) and [DyIII(acac)3(tmphen)]·2H2O (2) (tmphen = 3,4,7,8-tetramethyl-1,10-phenanthroline, hfac = hexafluoroacetylacetone, acac = acetylacetone) have been synthesized and structurally characterized by single crystal X-ray diffraction. Magnetic properties indicate that both of the complexes exhibit SMM behavior, and complex 1 is the first typical derivative of phenanthroline containing D2d-Dy(iii) based mononuclear single molecule magnets. The energy barrier (Ueff/kB) of complex 2 (130.42 K) is much higher than that of complex 1 (35.09 K), indicating that the local symmetry of Dy(iii) ions (D2d for 1, D4d for 2) plays an important role in magnetic behaviors.
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 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