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Quantitative affinity cleavage

The initiation reaction comprises the nucleophihc attack of the initiator at the carbonyl carbon, followed by an acyl-oxygen cleavage and formation of the active species, an alcoholate [24]. The efficiency of the initiation depends on the nucleophi-Hcity of the initiator and on the electron affinity of the monomer if both are high, then initiation is both fast and quantitative. A slow initiation leads to a broadening of the molecular weight distribution and a loss of molecular weight control. [Pg.309]


See other pages where Quantitative affinity cleavage is mentioned: [Pg.276]    [Pg.276]    [Pg.616]    [Pg.301]    [Pg.122]    [Pg.213]    [Pg.57]    [Pg.73]    [Pg.351]    [Pg.1059]    [Pg.509]    [Pg.140]    [Pg.242]    [Pg.460]    [Pg.19]    [Pg.218]    [Pg.334]    [Pg.232]    [Pg.483]    [Pg.220]    [Pg.353]    [Pg.2706]    [Pg.2714]    [Pg.3959]    [Pg.4924]    [Pg.670]    [Pg.50]    [Pg.247]    [Pg.290]    [Pg.315]    [Pg.255]    [Pg.26]    [Pg.1191]   
See also in sourсe #XX -- [ Pg.276 ]




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Affinity cleavage

Quantitating Affinity

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