1273-86-5, Name is Ferrocenemethanol, belongs to iron-catalyst compound, is a common compound. HPLC of Formula: C11H3FeOIn an article, once mentioned the new application about 1273-86-5.
One-electron oxidation of ferrocenes by short-lived N-oxyl radicals. the role of structural effects on the intrinsic electron transfer reactivities
A kinetic study of the one electron oxidation of substituted ferrocenes (FcX: X = H, COPh, COMe, CO2Et, CONH2, CH2OH, Et, and Me2) by a series of N-oxyl radicals (succinimide-N-oxyl radical (SINO), maleimide-N-oxyl radical (MINO), 3-quinazolin-4-one-N-oxyl radical (QONO) and 3-benzotriazin-4-one-N-oxyl radical (BONO)), has been carried out in CH3CN. N-oxyl radicals were produced by hydrogen abstraction from the corresponding N-hydroxy derivatives by the cumyloxyl radical. With all systems, the rate constants exhibited a satisfactory fit to the Marcus equation allowing us to determine self-exchange reorganization energy values (lambdaNO/NO-) which have been compared with those previously determined for the PINO/PINO- and BTNO/BTNO- couples. Even small modification of the structure of the N-oxyl radicals lead to significant variation of the lambdaNO/NO- values. The lambdaNO/NO- values increase in the order BONO < BTNO < QONO < PINO < SINO < MINO which do not parallel the order of the oxidation potentials. The higher lambdaNO/NO- values found for the MINO and SINO radicals might be in accordance with a lower degree of spin delocalization in the radicals MINO and SINO and charge delocalization in the anions MINO- and SINO- due to the absence of an aromatic ring in their structure.
One-electron oxidation of ferrocenes by short-lived N-oxyl radicals. the role of structural effects on the intrinsic electron transfer reactivities
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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