Abstract
In this work, we report the generation and characterization of two new Co(III)-peroxo complexes 2 and 3. 2 is best described as a mononuclear CoIII-(O2) complex that exhibits an 18O-isotope sensitive O–O bond stretching vibration at 845(−49) cm−1, indicating a relatively weak peroxo moiety compared to those of other CoIII-(O2) complexes reported previously. Complex 3 is a CoIII-peroxo-arylboronate species having a rare {CoIIIOOBO} five-membered metallocycle, which is structurally characterized using X-ray crystallography. Investigations of the reaction mechanism using density functional theory calculations show that 2 likely undergoes a nucleophilic attack to an arylboronic acid, which is generated by hydrolysis of the BPh4− anion in wet acetonitrile solution, to first form a CoIII-peroxo-arylboronic acid adduct, followed by the loss of one benzene molecule to generate the five-membered metallocycle. The entire reaction is thermodynamically favorable. Taken together, the conversion of 2 to 3 represents the discovery of a novel nucleophilic reactivity that can be carried out by mononuclear Co(III)-peroxo complexes.
| Original language | English |
|---|---|
| Article number | 112552 |
| Pages (from-to) | 112552 |
| Journal | Journal of Inorganic Biochemistry |
| Volume | 256 |
| DOIs | |
| State | Published - Jul 2024 |
Keywords
- Cobalt-peroxo-arylboronate species
- Five-membered metallocycle
- Mononuclear metal-peroxo species
- Nucleophilic reaction
- Side-on cobalt-peroxo complex
- Cobalt/chemistry
- Boronic Acids/chemistry
- Crystallography, X-Ray
- Molecular Structure
- Coordination Complexes/chemistry
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