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Isolable zwitterionic pyridinio-semiquinone pi-radicals. Mild and efficient single-step access to stable radicals.
Yi, Chenyi; Blum, Carmen; Liu, Shi-Xia; Keene, Tony D; Frei, Gabriela; Neels, Antonia; Decurtins, Silvio.
Affiliation
  • Yi C; Departement für Chemie und Biochemie, Universität Bern, Freiestrasse 3, CH-3012 Bern, Switzerland.
Org Lett ; 11(11): 2261-4, 2009 Jun 04.
Article in En | MEDLINE | ID: mdl-19402676
ABSTRACT
A rational design based on the proton-coupled electron transfer (PCET) concept allows us to structurally characterize for the first time isolable, air- and moisture-stable semiquinone radicals in a zwitterionic neutral form. The presence of an alkoxy and the bulky pyridinio substituents causes only a minor perturbation of either the redox potentials or the spectral UV-vis characteristics of the semiquinone core but significantly stabilizes the new radicals.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Pyridines / Benzoquinones Language: En Journal: Org Lett Journal subject: BIOQUIMICA Year: 2009 Document type: Article Affiliation country: Switzerland Publication country: EEUU / ESTADOS UNIDOS / ESTADOS UNIDOS DA AMERICA / EUA / UNITED STATES / UNITED STATES OF AMERICA / US / USA

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Pyridines / Benzoquinones Language: En Journal: Org Lett Journal subject: BIOQUIMICA Year: 2009 Document type: Article Affiliation country: Switzerland Publication country: EEUU / ESTADOS UNIDOS / ESTADOS UNIDOS DA AMERICA / EUA / UNITED STATES / UNITED STATES OF AMERICA / US / USA