Intercepting a transient non-hemic pyridine N-oxide Fe(iii ) species involved in OAT reactions
Author(s) -
Nhat Tam Vo,
Christian Herrero,
Régis Guillot,
Tanya Inceoglu,
Winfried Leibl,
Martin Clémancey,
Patrick Dubourdeaux,
Geneviève Blondin,
Ally Aukauloo,
Marie Sircoglou
Publication year - 2021
Publication title -
chemical communications
Language(s) - Uncategorized
Resource type - Journals
SCImago Journal Rank - 1.837
H-Index - 333
eISSN - 1364-548X
pISSN - 1359-7345
DOI - 10.1039/d1cc04521k
Subject(s) - catalysis , context (archaeology) , chemistry , ligand (biochemistry) , electron paramagnetic resonance , pyridine , transient (computer programming) , derivative (finance) , crystallography , medicinal chemistry , biochemistry , nuclear magnetic resonance , biology , receptor , physics , paleontology , computer science , financial economics , economics , operating system
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, Mössbauer, 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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