Compound, resin, composition, and method for forming pattern
A compound and carbon number technology, applied in organic chemistry, photoengraving process of pattern surface, coating, etc., can solve the problems of resist pattern collapse, resolution problem, difficulty in obtaining resist pattern, etc.
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[0858] Hereinafter, this embodiment will be described in more detail based on synthesis examples and examples, but this embodiment is not limited to these examples at all.
[0859] (carbon concentration and oxygen concentration)
[0860] Carbon concentration and oxygen concentration (mass %) were measured by organic elemental analysis.
[0861] Device: CHN CORDER MT-6 (manufactured by Yanac Analytical Industry Co., Ltd.)
[0862] (molecular weight)
[0863] The molecular weight of the compound was measured by LC-MS analysis using Acquity UPLC / MALDI-Synapt HDMS manufactured by Water Corporation.
[0864] In addition, gel permeation chromatography (GPC) analysis was carried out under the following conditions to obtain polystyrene-equivalent weight average molecular weight (Mw), number average molecular weight (Mn), and degree of dispersion (Mw / Mn).
[0865]Device: Shodex GPC-101 (manufactured by Showa Denko Co., Ltd.)
[0866] Column: KF-80M×3
[0867] Eluent: THF 1mL / min ...
Synthetic example 1A
[0879] Synthesis of E-XBisN-1
[0880] In a container with an internal volume of 100 ml equipped with a stirrer, a condenser and a burette, 10 g (21 mmol) of the compound (XBisN-1) shown in the above formula and 14.8 g (107 mmol) of potassium carbonate were dropped into 50 ml of dimethylformamide, 6.56 g (54 mmol) of 2-chloroethyl acetate was added, and the reaction solution was stirred at 90° C. for 12 hours to react. Next, the reaction solution was cooled in an ice bath to precipitate crystals, which were filtered and separated. Next, 40 g of the aforementioned crystals, 40 g of methanol, 100 g of THF and 24% aqueous sodium hydroxide solution were put into a container with an inner volume of 100 ml including a stirrer, a condenser, and a burette, and the reaction solution was stirred under reflux for 4 hours to react. Thereafter, the mixture was cooled in an ice bath, the reaction solution was concentrated, and the precipitated solid was filtered and dried, followed by sep...
Synthetic example 2A
[0892] 11.2 g (21 mmol) of the compound (BisF-1) represented by the above formula and 14.8 g (107 mmol) of potassium carbonate were added to 50 ml of dimethylformamide in a container with an internal volume of 100 ml including a stirrer, a condenser, and a burette. , 6.56 g (54 mmol) of 2-chloroethyl acetate was added, and the reaction solution was stirred at 90° C. for 12 hours to react. Next, the reaction solution was cooled in an ice bath to precipitate crystals, which were filtered and separated. Next, 40 g of the aforementioned crystals, 40 g of methanol, 100 g of THF and 24% aqueous sodium hydroxide solution were put into a container with an inner volume of 100 ml including a stirrer, a condenser, and a burette, and the reaction solution was stirred under reflux for 4 hours to react. Thereafter, it was cooled in an ice bath, the reaction solution was concentrated, and the precipitated solid was filtered and dried, followed by separation and purification by column chromat...
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