Because a catalyst decreases the height of the energy barrier, Recommanded Product: Bis(acetylacetone)copper, its presence increases the reaction rates of both the forward and the reverse reactions by the same amount.Recommanded Product: Bis(acetylacetone)copper, Name is Bis(acetylacetone)copper, molecular formula is C10H16CuO4. In a article£¬once mentioned of Recommanded Product: Bis(acetylacetone)copper
Binuclear copper complexes with CuICuI and Cu+1.5Cu+1.5 core structures formed in the reactions of 3?(2?methylbutyl)?5?pyridylmethylene?2?thiohydantoin with copper(II) acetylacetonate and copper(II) chloride
A treatment of the ligands, 3?(2?methylbutyl)?5?pyridylmethylene-substituted 2?thio?3,5?dihydro?4??imidazole?4?one (L) with CuCl2¡¤2H2O in MeOH/CH2Cl2 or Cu(acac)2 in MeOH/CH2Cl2 affords to binuclear complexes with the [L-H]2Cu+1.5Cu+1.5Cl or [L-H]2CuICuI composition, respectively. X-ray crystallography demonstrated close Cu-Cu interaction for the first complex and the absence of Cu?Cu bonding for the second one.
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 13395-16-9
Reference£º
Copper catalysis in organic synthesis – NCBI,
Special Issue “Fundamentals and Applications of Copper-Based Catalysts”