Abstract
The electrochemical one-electron reduction of IDipp·N2O (IDipp = 1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene) is inherently irreversible, highlighting the short-lived nature of the corresponding radical anion. However, stabilization by Lewis acidic boranes enables electrochemically reversible behavior, unlocking access to persistent radical species. These radicals are synthesized via chemical reduction and fully characterized, revealing a highly N-centered nature alongside remarkable persistence at room temperature under an inert atmosphere. A comprehensive investigation of their electronic structure is presented, integrating electron paramagnetic resonance techniques (both continuous-wave and pulsed) with theoretical analysis to provide deeper insight into their properties.
| Original language | English |
|---|---|
| Pages (from-to) | 2140-2147 |
| Number of pages | 8 |
| Journal | Chemical Science |
| Volume | 17 |
| Issue number | 4 |
| DOIs | |
| State | Published - Jan 28 2026 |
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