Synthetic Route of 1273-94-5, Because a catalyst decreases the height of the energy barrier, its presence increases the reaction rates of both the forward and the reverse reactions by the same amount.1273-94-5, Name is 1,1′-Diacetylferrocene, molecular formula is C14H6FeO2. In a article£¬once mentioned of 1273-94-5
Synthesis and biological properties of Cu(II) complexes with 1,1?-disubstituted ferrocenes
1,1?-Disubstituted ferrocenes have been prepared and used as chelating ligands in the preparation of Cu(II) compounds with a variety of anions such as nitrate, sulfate, oxalate, and acetate. These compounds have been characterized by physical, spectral, and analytical methods. Screening of these derivatives against pathogenic bacterial species such as Staphylococcus aureus, Escherichia coli, Pseudomonas aeruginosa, and Klebsiella pneumoniae showed all of them to possess varied bactericidal activity.
Synthesis and biological properties of Cu(II) complexes with 1,1?-disubstituted ferrocenes
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 1273-94-5
Reference£º
Iron Catalysis in Organic Synthesis | Chemical Reviews,
Iron Catalysis in Organic Synthesis: A Critical Assessment of What It Takes To Make This Base Metal a Multitasking Champion