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Coordinated ligands, chirality polymerization mechanisms

Rh138 was almost the same (almost atactic, slightly syndiotactic) as the tacticity of those obtained with conventional radical initiators such as AIBN under similar conditions. The triad ratio of rr.mr.mm as determined by 13C NMR is usually 58 38 4 and does not change even with the use of chiral and/or bulky ligands.103116 These results may exclude a coordination mechanism and suggest a radical nature. However, the stereochemical structure alone is not strong evidence for the radical polymerization because, for example, group-transfer polymerization, basically via an anionic mechanism, results in a stereo structure of PMMA similar to those for free radical processes.263... [Pg.480]


See other pages where Coordinated ligands, chirality polymerization mechanisms is mentioned: [Pg.68]    [Pg.206]    [Pg.76]    [Pg.114]    [Pg.55]    [Pg.260]    [Pg.669]    [Pg.787]    [Pg.856]    [Pg.1019]    [Pg.1020]    [Pg.669]    [Pg.204]    [Pg.22]    [Pg.167]    [Pg.101]    [Pg.76]    [Pg.246]   
See also in sourсe #XX -- [ Pg.9 ]




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Chiral coordination

Chiral ligands

Chiral mechanisms

Coordinated ligands, chirality polymerization

Coordination mechanism

Coordination polymerization

Ligand coordination

Ligand mechanisms

Ligands chirality

Mechanism coordination polymerization

Polymeric Ligands

Polymeric chiral

Polymerization coordinated

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