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Fluorinated PAE

Ethynyl terminated fluorinated PAES has a potential use for optical waveguide applications. The synthesis of ethynyl terminated fluorinated PAES is shown in Figure 7.12. The polymer is cured at 270°C for 2 h. [Pg.267]

A bisphenol monomer, 2,2 -dimethylaminemethy-lene-4,4 -biphenol has been prepared by the Mannich reaction of dimethylamine and formaldehyde with 4,4 -biphenol. This monomer can be used for the synthesis of partially fluorinated PAES polymers with pendant quaternary anunonium groups. The synthesis is shown in Figure 7.2. [Pg.180]

Quatemized PAES with up to two pendant quaternary ammonium groups have been prepared by a cesium carbonate mediated direct aromatic nucleophihc subshtuhon polycondensahon of 2,2 -dimethylaminemethylene-4,4 -biphenol, 4,4 -biphenol, and 4,4 -difluorodiphenyl sulfone, followed by the reaction with iodomethane [96]. These types of ionomers are more stable than some fluorinated PAES ionomers under highly basic conditions. [Pg.192]

Fluorinated PAEs with Terphenyl, Pyridinylidene, Thiophenylidene,... [Pg.11]

Fluorinated PAEs with Anthracene and Fluorene Moieties... [Pg.22]

Fluorinated PAEs with Naphthyl and Naphthyl-lmido Moiety... [Pg.25]

Ueda et al. [63] synthesized a fluorinated PAE containing naphthalene moiety and investigated its properties. The polymer was synthesized by catalytic oxidative coupling polymerization using FeCls (Scheme 2.13). The polymer had an Mn of 32,000g/ mol with good film processability. The polymer had a Tg value of 230 °C and was recorded at 530 °C. [Pg.26]

Fluorinated PAEs with Cardo Cyclohexylidene Moiety... [Pg.28]

Fluorinated PAEs with Phenyl Phosphine Oxide Moiety... [Pg.28]

Kim and coworkers [137] prepared sulfonated fluorinated PAEs containing naphthalene moieties in the main chain (SPAE-XX, where XX = 20,30,40,50,60, 70, and 80) with DS=0.2, 0.3, 0.4, 0.5, 0.6, 0.7, and 0.8. The sulfonic acid groups were a bonded meta- to et/ier-linkage of a naphthalene ring in the polymer. The -CF3 groups were introduced into the polymer structure by using 6F-BPA units that controlled the sulfonic acid content in the copolymer composition. [Pg.58]


See other pages where Fluorinated PAE is mentioned: [Pg.11]    [Pg.11]    [Pg.11]    [Pg.11]    [Pg.11]    [Pg.11]    [Pg.11]    [Pg.11]    [Pg.11]    [Pg.11]    [Pg.11]    [Pg.11]    [Pg.11]    [Pg.18]    [Pg.25]    [Pg.25]    [Pg.26]    [Pg.28]    [Pg.29]    [Pg.29]    [Pg.30]    [Pg.31]    [Pg.39]    [Pg.40]    [Pg.40]    [Pg.41]    [Pg.41]    [Pg.41]    [Pg.53]    [Pg.54]    [Pg.54]    [Pg.57]    [Pg.62]    [Pg.62]    [Pg.66]    [Pg.68]    [Pg.70]    [Pg.72]    [Pg.73]   
See also in sourсe #XX -- [ Pg.54 , Pg.55 ]




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Densely sulfonated fluorinated PAEs

PAE

Sulfonated fluorinated PAEs

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