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Electron 2,3-dichloro-5,6-dicyanobenzoquinone

Particular attention is deserved for the paper by Miller and co-workers describing the new procedure for the synthesis and characterization of cyanil (35) as the strongest isolated electron acceptor and its reduced forms [55], The synthesis was carried out in a three-step procedure from commercially available p-bromanil or 2,3-dichloro-5,6-dicyanobenzoquinone (DDQ) and methanolic NaCN to form the tetracyanohydroquinone which was transformed into the insoluble disilver salt by treatment with silver nitrate followed by bromine oxidation to yield cyanil as a yellow crystalline material. [Pg.14]


See other pages where Electron 2,3-dichloro-5,6-dicyanobenzoquinone is mentioned: [Pg.6]    [Pg.10]    [Pg.319]    [Pg.251]    [Pg.324]    [Pg.324]    [Pg.331]    [Pg.100]    [Pg.661]    [Pg.192]    [Pg.4]    [Pg.242]    [Pg.328]    [Pg.181]    [Pg.133]    [Pg.1508]   


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Dicyanobenzoquinone

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