Abstract
We demonstrate that the reactions of [FeIII(η2-O2)(TMC)]+ (TMC = tetramethylcyclam) with Lewis acids (H+ and NO+) afford the recently described syn isomer of [FeIV(O)(TMC)(NCMe)]2+ (and not the anti isomer as had been tacitly assumed). This outcome is a logical consequence of the fact that the side-on peroxo ligand is bound to the syn face of the Fe(TMC) unit in the precursor.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 8146-8148 |
| Number of pages | 3 |
| Journal | Chemical Communications |
| Volume | 52 |
| Issue number | 52 |
| DOIs | |
| State | Published - 2016 |
Bibliographical note
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