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Biomimetic oxidations at active sites of iron proteins involve peroxides, especially hydrogen peroxide which is a strong and very convenient reagent since it is inexpensive and does not release any toxic by-products. In many cases however, mother N ature uses molecular dioxygen to carry out major oxidation reactions in particularly attractive conditions. The biomimetic interest of iron complexes in the tris(2-pyridylmethyl)amine series TPA is no longer to demonstrate. We prepared various α-substituted TPA-based ligands with the idea to modulate the electronic properties at the metal centre. We then checked the reactivity of a one example of complexes towards molecular dioxygen.
The possibility of formating a colored complex between Fe2+ ions and 4-Hydroxy-3- [[(2-hydroxy phenyl) methylene] amino] benzene Sulphonic Acid (HVMAB) was studied spectrophotometric method for determination of iron in aqueous solutions. The reagen t reacts in aqueous medium at pH=5 to give an orange complex with maximum absorbance λmax=415nm.
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