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Higher phenylenes, synthesis

Polymerization in a single-phase homogeneous solution in THF/water mixtures (2 1) has also been reported [235]. Such reactions allowed for the preparation of a poly (p-phenylene) with sulfonate ester and dodecyl side groups [Eq. (10)]. By comparison to the aforementioned biphasic polymerizations, the synthesis of polymers with higher degrees of polymerization was reported in the solution procedure. [Pg.267]

A degree of compatibility between polymers is introduced by IPN formation as two polymers are interlocked in a three-dimensional structure during synthesis. The phase domains are smaller in higher compatibility systems. Most of the early IPN studies were based on immiscible polymers and a small gain in phase mixing was observed. Frisch and coworkers prepared IPNs from PS and poly(2,6-dimethyl-l,4-phenylene oxide), which were miscible. Klempner prepared IPNs that contained opposite charges, and showed better miscibility than IPNs without charge. [Pg.34]


See other pages where Higher phenylenes, synthesis is mentioned: [Pg.145]    [Pg.241]    [Pg.331]    [Pg.486]    [Pg.132]    [Pg.233]    [Pg.55]    [Pg.90]    [Pg.221]    [Pg.6]    [Pg.331]    [Pg.63]    [Pg.241]    [Pg.303]    [Pg.241]    [Pg.304]    [Pg.193]    [Pg.417]    [Pg.28]    [Pg.360]    [Pg.241]    [Pg.21]    [Pg.133]    [Pg.5]    [Pg.319]    [Pg.331]    [Pg.247]    [Pg.46]    [Pg.141]    [Pg.141]    [Pg.414]    [Pg.96]    [Pg.4]    [Pg.13]    [Pg.70]    [Pg.323]    [Pg.382]    [Pg.611]    [Pg.420]    [Pg.397]    [Pg.6]    [Pg.88]    [Pg.5926]    [Pg.2151]    [Pg.2383]    [Pg.4103]    [Pg.263]    [Pg.156]   
See also in sourсe #XX -- [ Pg.145 ]




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Phenylene synthesis

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