Intercepting a transient non-hemic pyridine N-oxide Fe(III) species involved in OAT reactions
Résumé
In the context of bioinspired OAT catalysis, we developed a tetradentate dipyrrinpyridine ligand, a hybrid of hemic and non-hemic models. The catalytic activity of the iron(iii) derivative was investigated in the presence of iodosylbenzene. Unexpectedly, MS, EPR, Mossbauer, UV-visible and FTIR spectroscopic signatures supported by DFT calculations provide convincing evidence for the involvement of a relevant Fe-III-O-N-Py active intermediate.
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