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Carbanion basicity

Neutral organic molecules can also be one-electron donors. For example, tetracyano-quinodimethane gives rise to anion-radical on reduction with 10-vinylphenothiazine or N,N,N, N -tetramethyl-p-phenylenediamine. Sometimes, alkoxide or phenoxide anions hnd their applications as one-electron donors. There is a certain dependence between carbanion basicity and their ability to be one-electron donors (Bordwell and Clemens 1981). [Pg.88]

Structural Effects on Carbanion Basicity-Carbon Acidity... [Pg.79]

See other pages where Carbanion basicity is mentioned: [Pg.72]    [Pg.210]    [Pg.148]   
See also in sourсe #XX -- [ Pg.369 , Pg.593 ]

See also in sourсe #XX -- [ Pg.369 , Pg.593 ]

See also in sourсe #XX -- [ Pg.369 , Pg.593 ]

See also in sourсe #XX -- [ Pg.345 , Pg.552 ]



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Basicity Carbanions

Basicity properties, carbanions

Carbanions basic principles

Carbanions basicity, relative

Carbon acidity, carbanion basicity condensed-phase measurements

Generation of Stabilized Carbanions Under Basic Conditions

Structural Effects on Carbanion Basicity-Carbon Acidity

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