Ink repellent composition, negative photosensitive resin composition, cured film, partition wall, and optical element
A technology of photosensitive resin and composition, which is applied in the direction of optics, electrical components, electric solid devices, etc., can solve the problems of insufficient use of partition walls of organic EL components, etc., and achieve the effect of good UV/O3 resistance and easy formation
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[0405] The present invention is explained based on examples, and the present invention is not limitedly interpreted by them. Examples 1-10, Example 14 and Example 15 are examples, and Examples 11-13 are comparative examples.
[0406] Each measurement was performed by the following method.
[0407] [Number average molecular weight (Mn) and mass average molecular weight (Mw)]
[0408]The number average molecular weight (Mn) and the mass average molecular weight (Mw) were measured by gel permeation chromatography using polystyrene as a standard substance. As the gel permeation chromatography, HPLC-8220GPC (manufactured by Tosoh Corporation) was used. As the column, a column obtained by connecting three Shodex LF-604 pieces was used. As a detector, an RI (Refractive Index, refractive index) detector is used. As a standard substance, EasiCal PS1 (manufactured by Polymer Laboratories) was used. Furthermore, when measuring the number average molecular weight and mass average mol...
Synthetic example 1
[0466] [Synthesis Example 1: Synthesis of Compound (CX-1)]
[0467] At 1,000cm equipped with a mixer 3 Put compound (cx-11) 14.5g, compound (cx-21) 32.9g, compound (cx-31) 21.9g, compound (cx-41) 21.9g, and compound (cx-51) 8.8g into a three-necked flask , to obtain a hydrolyzable silane compound mixture. Next, 320.2 g of PGMEA was thrown into this mixture to prepare a raw material solution.
[0468] 98.7 g of 1 mass % nitric acid aqueous solution was dripped at the obtained raw material solution. After completion of the dropwise addition, it was stirred at 40° C. for 5 hours to obtain a solution of compound (CX-1) (compound concentration: 10% by mass, hereinafter also referred to as (CX-1) solution.).
[0469] It should be noted that after the reaction was completed, the reaction solution was measured using a gas chromatograph, and it was confirmed that each compound used as a raw material was below the detection limit.
[0470] Table 1 shows the raw material composition ...
Synthetic example 2~6
[0471] [Synthesis Examples 2 to 6: Compounds (CX-2) to (CX-6)]
[0472] Except that the raw material composition was set as shown in Table 1, the same operation was performed as in Synthesis Example 1 to obtain solutions of compounds (CX-2) to (CX-6) (both compound concentrations: 10% by mass, and each solution was also hereinafter referred to as Called (CX-2) ~ (CX-6) liquid.).
[0473] Table 1 shows the evaluation results (number average molecular weight (Mn), mass average molecular weight (Mw), fluorine atom content, and ethylenic double bond content).
[0474] [Table 1]
[0475]
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