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Poly ether sulfonejs

The SnAt reactions were first successfully used in the synthesis of high-molecular-weight poly(arylene etherjs by Johnson et al.4,5 This reaction represents a good example for poly(ether sulfonejs in general, either in laboratory -or industrial-scale preparations. In this procedure, the bisphenol A and sodium hydroxide with an exact mole ratio of 1 2 were dissolved into dimethyl sulfoxide (DMSO)-chlorobenzene. The bisphenol A was converted into disodium bisphenolate A, and water was removed by azeotropic distillation. After the formation of the anhydrous disodium bisphenolate A, an equal molar amount of 4,4,-dichlorodiphenyl sulfone (DCDPS) was added in chlorobenzene under anhydrous conditions and the temperature was increased to 160°C for over 1 h... [Pg.336]

Table 7.4 Major Products of Pyrolysis of Poly(ether sulfonejs... Table 7.4 Major Products of Pyrolysis of Poly(ether sulfonejs...
In poly(ether sulfonejs that are prepared by polycondensation of silylated 4-tert-butylcatechol and 4,4 -difluorodiphenyl sulfone, macrocyclic polymers were obtained to some extent [10]. The cyclic polymers were detected by means of matrix-assisted laser desorption ionization time-of-flight (MALDI-TOF) mass spectrometry. [Pg.184]


See other pages where Poly ether sulfonejs is mentioned: [Pg.347]   
See also in sourсe #XX -- [ Pg.33 , Pg.60 ]




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