Effects of a Hydroxyl Substituent on the Reactivity of the 2,4,6-Tridehydropyridinium Cation, an Aromatic σ,σ,σ-Triradical-Reference-Cited by-同舟云学术

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Effects of a Hydroxyl Substituent on the Reactivity of the 2,4,6-Tridehydropyridinium Cation, an Aromatic σ,σ,σ-Triradical

Published:2011-12-16 Issue:3 Volume:18 Page:969-974
ISSN:0947-6539
Container-title:Chemistry - A European Journal
language:en
Short-container-title:Chem. Eur. J.

Author:

Jankiewicz Bartłomiej J.,Vinueza Nelson R.,Reece Jennifer N.,Lee Young C.,Williams Peggy,Nash John J.,Kenttämaa Hilkka I.

Publisher

Wiley

Subject

General Chemistry,Catalysis,Organic Chemistry

Reference58 articles.

1. Electronic structure of the 1,3,5-tridehydrobenzene triradical in its ground and excited states

2. Bonding Patterns in Benzene Triradicals from Structural, Spectroscopic, and Thermochemical Perspectives

4. Energetics and chemical bonding of the 1,3,5-tridehydrobenzene triradical and its protonated form

5. The 1,2,3-Tridehydrobenzene Triradical: 2B or Not 2B? The Answer is 2A!

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1. Spin‐Spin Coupling between the Biradical Moieties in Aromatic Tetraradicals Increases their Reactivity;Israel Journal of Chemistry;2023-07-04

2. Spin‐Spin Coupling Controls the Gas‐Phase Reactivity of Aromatic σ‐Type Triradicals;Chemistry – A European Journal;2021-12-06

3. Quinoline Triradicals: A Reactivity Study;Journal of the American Chemical Society;2019-04-04

4. Spin–Spin Coupling Between Two meta ‐Benzyne Moieties In a Quinolinium Tetraradical Cation Increases Their Reactivities;Chemistry – A European Journal;2019-02-25

5. Substituent Effects on the Reactivity of the 2,4,6-Tridehydropyridinium Cation, an Aromatic σ,σ,σ-Triradical;European Journal of Organic Chemistry;2018-11-15

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