Compound, resin, composition, pattern forming method and purification method
A compound and carbon number technology, applied in the field of material purification, can solve the problems of resist pattern collapse, resolution problems, and difficulty in obtaining resist patterns, etc.
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[0490] Hereinafter, an Example is given and the embodiment of this invention is demonstrated more concretely. However, the present embodiment is not particularly limited to these examples.
[0491] The analysis and evaluation methods of the compounds are as follows.
[0492]
[0493] The molecular weight of the compound was measured by LC-MS analysis using Acquity UPLC / MALDI-Synapt HDMS manufactured by Water Corporation.
[0494]
[0495] Using an EXSTAR6000DSC device manufactured by SII NanoTechnology Inc., about 5 mg of the sample was placed in an aluminum non-sealed container, and the temperature was raised to 500°C at a heating rate of 10°C / min in a nitrogen (30ml / min) flow. At this time, the temperature at which a decrease in the base line appeared was taken as the thermal decomposition temperature.
[0496]
[0497] Using an EXSTAR6000DSC device manufactured by SII NanoTechnology Inc., about 5 mg of the sample was placed in an aluminum non-sealed container, and t...
manufacture example 1
[0530] A four-neck flask with an inner volume of 10 L whose bottom can be removed, equipped with a serpentine condenser, a thermometer, and a stirring blade, was prepared. In this four-necked flask, 1.09 kg (7 mol, manufactured by Mitsubishi Gas Chemical Co., Ltd.) of 1,5-dimethylnaphthalene and 2.1 kg of 40% by mass formalin aqueous solution (28 mol as formaldehyde) were charged in a nitrogen stream. , manufactured by Mitsubishi Gas Chemical Co., Ltd.) and 0.97 mL of 98% by mass sulfuric acid (manufactured by Kanto Chemical Co., Ltd.), were reacted under normal pressure while refluxing at 100° C. for 7 hours. Thereafter, 1.8 kg of ethylbenzene (special grade, manufactured by Wako Pure Chemical Industries, Ltd.) was added as a diluting solvent to the reaction solution, and the lower aqueous phase was removed after standing still. Further, neutralization and water washing were performed, and ethylbenzene and unreacted 1,5-dimethylnaphthalene were distilled off under reduced pre...
Embodiment 1~20
[0533] Table 3 shows the results of evaluating the solubility to propylene glycol monomethyl ether (PGME) using BisP-1 to BisP-18, R1-BisP-1, and R2-BisP-2.
[0534] [table 3]
[0535] table 3
[0536] compound Solubility evaluation results Example 1 BisP-1 A Example 2 BisP-2 A Example 3 BisP-3 A Example 4 BisP-4 A Example 5 BisP-5 A Example 6 BisP-6 A Example 7 BisP-7 A Example 8 BisP-8 A Example 9 BisP-9 A Example 10 BisP-10 A Example 11 BisP-11 A Example 12 BisP-12 A Example 13 BisP-13 A Example 14 BisP-14 A Example 15 BisP-15 A Example 16 BisP-16 A Example 17 BisP-17 A Example 18 BisP-18 A Example 19 R1-BisP-1 A Example 20 R2-BisP-1 A
[0537] From Table 3, it was clearly confirmed that the compounds used in Examples 1 to 20 were all excellent in solubility to solvents.
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