
Chemistry Letters p. 863 - 866 (1994)
Update date:2022-07-29
Topics:
Takahashi, Kazuko
Gunji, Atsushi
Akiyama, Kimio
Novel p-terphenoquinone analogues incorporating a central dihydrofurandiylidene skeleton have been synthesized.These quinones gave a stable radical kation and a stable radical anion on one-electron redox reactions showing an amphoteric property even though they do not contain any sulfur atom as an integral component.The radical cation and the radical anion of the tetra-t-butyl derivative have been characterized by EPR spectroscopy.
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