Singlet oxygen-mediated selective C-H bond hydroperoxidation of ethereal hydrocarbons.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 29180784.
- Also identified by DOI 10.1038/s41467-017-01906-5 and PMC identifier 5703888.
- Licence recorded as CC BY.
- The licence permits redistribution, so the abstract is shown in full and the full text is available from the publisher.
Abstract
Singlet O<sub>2</sub> is a key reactive oxygen species responsible for photodynamic therapy and is generally recognized to be chemically reactive towards C=C double bonds. Herein, we report the hydroperoxidation/lactonization of α-ethereal C-H bonds by singlet O<sub>2</sub> (<sup>1</sup>Δ<sub>g</sub>) under exceptionally mild conditions, i.e., room temperature and ambient pressure, with modest to high yields (38~90%) and excellent site selectivity. Singlet O<sub>2</sub> has been known for > 90 years, but was never reported to be able to react with weakly activated C-H bonds in saturated hydrocarbons. Theoretical calculations indicate that singlet O<sub>2</sub> directly inserts into the α-ethereal C-H bond in one step with conservation of steric configuration in products. The current discovery of chemical reaction of singlet oxygen with weakly activated solvent C-H bonds, in addition to physical relaxation pathway, provides an important clue to a 35-year-old unresolved mystery regarding huge variations of solvent dependent lifetime of singlet O<sub>2</sub>.