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Tetracyanobenzoquinone

Tetracyanobenzoquinone [4032-03-5] 3,6-dioxo-l,4-cyclohexadiene-l,2,4,5-tetracarbonitrile, is a remarkably strong oxidizing agent for a quinone it abstracts hydrogen from tetralin or ethanol even at room temperature (50). It is a stronger TT-acid than TCNE because it forms more deeply colored TT-complexes with aromatic hydrocarbons. [Pg.405]

More complex pathways can be followed dependent on the structure of the hydride acceptor. For example, dihydroacridine reacts cleanly with 2,3,5,6-tetracyanobenzoquinone to generate a pyridin-ium/radical anion pair. ... [Pg.93]

Thus, a compound like tetracyanobenzoquinone will be a better charge transfer agent than quinone. [Pg.913]

See other pages where Tetracyanobenzoquinone is mentioned: [Pg.853]    [Pg.259]    [Pg.383]    [Pg.1001]    [Pg.790]    [Pg.853]    [Pg.853]    [Pg.259]    [Pg.383]    [Pg.1001]    [Pg.790]    [Pg.853]   
See also in sourсe #XX -- [ Pg.5 ]

See also in sourсe #XX -- [ Pg.853 , Pg.854 ]



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Acridine, dihydrohydride transfer with 2,3,5,6-tetracyanobenzoquinone

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