Cross-linkable fluorinated photopolymer
A technology of polymers and polymer chains, applied in the direction of photosensitive materials, optics, and optomechanical equipment used in optomechanical devices, can solve the problem that the materials and patterning methods of inorganic electronic devices are not compatible with bioelectronic materials and organic electronic materials Compatibility and other issues
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[0069] The preparation and polymerization of the above monomers can generally be accomplished using standard synthetic methods known to those skilled in the art. Some useful examples of making orthogonal photopolymers can be found in US Publication No. 2011 / 0159252, PCT Publication WO2012148884, and co-pending US Application Nos. 14 / 291692, 14 / 291767, 14 / 335406, and 14 / 539574, all of which The contents are incorporated herein by reference. Examples of preparation of polymers incorporating acid-catalyzed crosslinkable groups can be found in US Publication Nos. 2009 / 0263588, 2009 / 0130591, and 2002 / 0161068, the entire contents of which are incorporated herein by reference. Examples of fluorinated copolymers comprising cinnamate can be found in US 4,529,783.
[0070]The fluorinated photopolymer compositions of the present disclosure can be applied to a substrate using any method suitable for depositing photosensitive liquid materials. For example, the composition can be applied ...
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[0092] Photopolymer compositions 1 to 6
[0093] Synthesis of 2-Cinnamoyloxyethyl Methacrylate (Compound C-8)
[0094] A solution of 8.3 g (0.05 mol) of cinnamoyl chloride and 10 mL of dry dimethylacetamide was slowly added to a stirred solution of 6.5 g (0.05 mol) of 2-hydroxyethyl methacrylate and 14 mL of dry pyridine under cooling in an ice bath middle. When the addition was complete, the cooling bath was removed and the mixture was allowed to warm to ambient temperature over 3 hours. Water and ethyl acetate were added to the reaction mixture and the product was extracted into the organic layer. The organic layer was washed successively with 1N hydrochloric acid solution, saturated sodium bicarbonate solution and saturated sodium chloride solution, then dried over magnesium sulfate, and filtered. The solvent was removed under vacuum to yield 12.1 g (93% of theoretical 13.0 g) of monomer as a clear yellow oil. The composition was verified using NMR. The monomer was...
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