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Updated: Jun 17, 2026

Isolating Free Carbenes, their Mixed Dimers and Organic Radicals
Published on: April 19, 2019
Redox-induced partner radical formation and its dynamic balance with radical dimer in cucurbit[8]uril
Tongyan Zhang1, Shiguo Sun, Fengyu Liu
1State Key Laboratory of Fine Chemicals, Dalian University of Technology, 158 Zhongshan Road, Xigang District, Dalian 116012, China.
Abstract:
N-(4-Hydroxy-phenoxyethyl)-N'-ethyl-4,4'-bipyridium (1) can form a stable 1 : 1 inclusion complex with CB[8] in aqueous solution, in which the hydroxyphenol (HP) moiety is back-folded and inserted together with the viologen moiety into the cavity of CB[8]. When the ethyl viologen dication (EV(2+)) in 1 is reduced, chemically or electrochemically, an intramolecular partner radical (EV(+)*-HP)/CB[8] can be detected, meanwhile, a dynamic balance between the partner radical and the intermolecular radical dimer (EV(+)*-HP)(2)/CB[8] can be observed.
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