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Oxyl radical configurations

TABLE 13. Ease of Oxyl Radical H Abstraction vs. Addition for Different Double Bond Configurations. Data from (279). [Pg.372]

Me and Ph are donors of electrons during addition the resonance effect prevails over polar one. Benzoyl-oxyl is an electron-acceptor radical the addition step is controlled merely by the polar effect [128]. During the addition of monomers to trimethylmethoxyl, both polar and resonance properties of their electron configuration are involved. [Pg.57]


See other pages where Oxyl radical configurations is mentioned: [Pg.197]    [Pg.337]    [Pg.145]    [Pg.164]    [Pg.646]    [Pg.122]    [Pg.136]    [Pg.140]   
See also in sourсe #XX -- [ Pg.329 ]




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Configuration radicals

Oxyl radical

Oxyls—

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