Photocurable polymers, photocurable polymer compositions and lithographic processes including the same
a technology of photocurable polymers and compositions, applied in the field of functionalized poly (aryl ether sulfones) polymers, can solve the problems of moderate mechanical properties and thermal stability of articles, and achieve the effects of high thermal properties, high tg, and high mechanical properties
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example 1
of PPSU with 4-Bromobutene (Invention)
[0116]This example demonstrates the synthesis of a functionalized PPSU polymer, more precisely functionalized with two terminal molecules according to the following scheme:
[0117]4,4′-dichlorodiphenyl sulfone (82.46 g, 0.287 mol), 4,4′-Biphenol (65.37 g, 0.351 mol), K2CO3 (50.95 g, 0.369 mol), and sulfolane (345 g) were combined in a 1 L 4-neck reaction vessel equipped with a mechanical stirrer, a Dean-Stark trap (wrapped in insulating cloth), an internal thermometer, and a nitrogen sparge tube. The resulting mixture was then slowly heated with stirring (45 min) to 210° C. and held at that temperature for 3.5 hours. Following build in molecular weight, the reaction mixture was then cooled to 90° C. and diluted with anhydrous NMP (about 230 mL) and K2CO3 was added (50 g). Following stirring for 15 minutes, 4-bromo-1-butene (112 g, 0.831 mol) was slowly injected via syringe and the resulting mixture was allowed to stir overnight at 100° C. To colle...
example 2
of PPSU with Vinyl Ether (Comparative)
[0119]This example demonstrates the synthesis of a functionalized PPSU polymer, more precisely functionalized with two terminal molecules according to the following scheme:
[0120]4,4′-dichlorodiphenyl sulfone (7.17 g, 0.025 mol), 4,4′-Biphenol (4.92 g, 0.0264 mol), K2CO3 (3.84 g, 0.028 mol), and sulfolane (28 g) were combined in a 200 mL 3-neck reaction vessel equipped with a mechanical stirrer, a Dean-Stark trap (wrapped in insulating cloth), an internal thermometer, and a nitrogen sparge tube. The resulting mixture was then slowly heated with stirring (45 min) to 210° C. and held at that temperature for 3.5 hours. Following build in molecular weight, the reaction mixture was then cooled to 95° C. and diluted with anhydrous NMP (about 20 g) and K2CO3 was added (3.83 g). Following stirring for 15 minutes, 2-chloroethyl vinyl ether (1.88 g, 0.0177 mol) was dissolved in anhydrous NMP (about 5 g) and slowly added to the reaction vessel via syringe. ...
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