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The First Heterotriquinone and Dicyanoheterotriquinone Methide That Undergo a Five-Stage Amphoteric Redox Reaction.
Takahashi, Kazuko; Fujita, Satoshi; Akiyama, Kimio; Miki, Misao; Yanagi, Kazunori.
Afiliação
  • Takahashi K; Department of Chemistry, Graduate School of Science Tohoku University, Sendai 980-8578 (Japan), Fax: (+81) 22-217-6560.
  • Fujita S; Department of Chemistry, Graduate School of Science Tohoku University, Sendai 980-8578 (Japan), Fax: (+81) 22-217-6560.
  • Akiyama K; Institute for Chemical Reaction Science, Tohoku University Sendai, 980-8577 (Japan).
  • Miki M; Biotechnology Laboratory, Sumitomo Chemical Co., Ltd. Takarazuka 665 (Japan).
  • Yanagi K; Biotechnology Laboratory, Sumitomo Chemical Co., Ltd. Takarazuka 665 (Japan).
Angew Chem Int Ed Engl ; 37(18): 2484-2487, 1998 Oct 02.
Article em En | MEDLINE | ID: mdl-29711367
ABSTRACT
The dicyanomethylene group and not the quinone oxygen atoms is the site of the first one-electron reduction for the dicyanohetereotriquinone methide 1, although the dicyanomethylene group is substituted at a cyclopentadienyl-like five-membered ring! Compound 1 is amphoteric and undergoes a five-stage sequence of one-electron redox reactions.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 1998 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 1998 Tipo de documento: Article