Is Electron Transfer a Step in the Nitration of Reactive Aromatics?
Controlled-potential electrolysis of a mixture of NO<sub>2</sub> and naphthalene, at an applied potential capable of oxidizing naphthalene but not NO<sub>2</sub>, produces a mixture of nitronaphthalenes. The ratio of 1-nitronaphthalene to 2-nitronaphthalene is 10.2 ± 1, the same as the 10.9 ± 1 produced in the direct nitration of naphthalene with HNO<sub>3</sub> + H<sub>2</sub>SO<sub>4</sub>. The observation that the same mixture is formed by the two routes is taken as evidence that a radical pair is involved not only in the electrochemical synthesis but also in the direct nitration. This requires that electron transfer from aromatic to NO<sub>2</sub><sup>+</sup> be sufficiently fast to compete with C-N bond formation. Moreover, formation of a radical pair is presented as the explanation for the high intramolecular selectivity of nitration, contrasting with a lack of intermolecular selectivity. This full paper presents the experimental details of a Communication to the Editor published in JACS in 1977, along with a review of experimental and computational assessments both in favor and in opposition to that Communication.
Authors
- Charles L. Perrin (ORCID: https://orcid.org/0000-0001-5732-5330)
Institutions
- University of California San Diego (US)
Publication Details
- Journal
- The Journal of Organic Chemistry
- Published
- 2026-02-17
- DOI
- https://doi.org/10.1021/acs.joc.5c03251
- Primary Topic
- Ammonia Synthesis and Nitrogen Reduction
- Type
- article
- Field-Weighted Citation Impact
- 0.00