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Dicyclic polymers

Alternatively, Tezuka et al. have proposed an electrostatic self-assembly and covalent fixation process for the effective synthesis of monocyclic and three dicyclic polymer structures [124,125]. The key reaction for formation of cyclic polymers is an electrostatic self-assembly and covalent fixation process, as indicated in Fig. 36. [Pg.156]

Scheme 1S.6 Click chemistry between a monocyclic prepolymer having an alkyne group and linear telechelic precursor with azide end groups, resulting in the selective formation of a fcndged-dicyclic manacle-shaped polymer. Scheme 1S.6 Click chemistry between a monocyclic prepolymer having an alkyne group and linear telechelic precursor with azide end groups, resulting in the selective formation of a fcndged-dicyclic manacle-shaped polymer.
A three-armed star telechelic precursor having cyclic ammonium salt groups has been prepared to form a self-assembly with one unit of tricarboxylate counteranion under dilution in order to keep the balance of the charges. The subsequent covalent fixation by heating produced a fused dicyclic, that is, 0-shaped, polymer effectively (Tezuka et al, 2003a). [Pg.15]


See other pages where Dicyclic polymers is mentioned: [Pg.534]    [Pg.534]    [Pg.535]    [Pg.535]    [Pg.537]    [Pg.1204]    [Pg.1204]    [Pg.1204]    [Pg.1204]    [Pg.534]    [Pg.534]    [Pg.535]    [Pg.535]    [Pg.537]    [Pg.1204]    [Pg.1204]    [Pg.1204]    [Pg.1204]    [Pg.886]    [Pg.538]    [Pg.15]    [Pg.16]    [Pg.17]    [Pg.18]   
See also in sourсe #XX -- [ Pg.534 ]




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