Chemically amplified resist compositon and pattern forming process
A composition and resist technology, which can be applied in the direction of optics, pattern-surface photoengraving process, opto-mechanical equipment, etc., and can solve problems such as affecting acid diffusion.
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Embodiment 1
[0121] Synthesis of Triphenylsulfonium Chloride
[0122] Dissolve 40 g (0.2 mol) of diphenylsulfoxide in 400 g of dichloromethane, and stir under ice cooling. At a temperature lower than 20° C., 65 g (0.6 mol) of trimethylsilyl chloride was added dropwise into the solution, and aged at this temperature for 30 minutes. Then, a Grignard reagent prepared from 14.6 g (0.6 mol) of magnesium metal, 67.5 g (0.6 mol) of chlorobenzene and 168 g of tetrahydrofuran (THF) was added dropwise at a temperature below 20°C. The reaction solution was allowed to mature for 1 hour, and then 50 g of water was added to quench the reaction at a temperature below 20°C. Further, 150 g of water, 10 g of 12N hydrochloric acid, and 200 g of diethyl ether were added to the solution. The aqueous layer was separated and washed with 100 g of diethyl ether to obtain an aqueous solution of triphenylsulfonium chloride. Compounds in aqueous solution were used in subsequent reactions without further isolation....
Embodiment 2
[0124] Synthesis of 4-tert-butylphenyldiphenylsulfonium bromide
[0125] The target compound was obtained according to the preparation method of Synthesis Example 1, except that 4-tert-butylbromobenzene was used instead of chlorobenzene in Synthesis Example 1 and the amount of water used for extraction was increased.
Embodiment 3
[0127] Synthesis of 4-tert-butoxyphenyldiphenylsulfonium chloride
[0128] In addition to replacing the chlorobenzene in Synthesis Example 1 with 4-tertiary oxychlorobenzene, using dichloromethane containing 5wt% triethylamine as a solvent, and increasing the amount of water used for extraction, the preparation according to Synthesis Example 1 Methods to obtain the target compound.
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