Coating compositions for use with overcoated photoresists
A technology of coating composition and photoresist, which is applied in the field of anti-reflection coating composition, planarization or via filling composition, and can solve problems such as pattern collapse and reduced depth of focus
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example 1
[0112] Example 1: Synthesis of Matrix Polymer 1
[0113] The polymer referred to herein as "Matrix Polymer 1" or simply "Polymer 1" was prepared in the following manner. 14g of 3,3'-(5-(2-(tert-butoxy)-2-oxoethyl)-2,4,6-trioxo-1,3,5-triazine-1,3-di base) dibutyl dipropionate, 27 g of tris-(2-hydroxyethyl) isocyanurate, a catalytic amount of p-toluenesulfonic acid monohydrate and 33 g of anisole were fed into the reactor. The reaction was heated and refluxed. After the reaction was completed, the reaction solution was cooled and diluted. The solution was added to a sufficient amount of alcoholic solvent and collected by filtration in a Buchner funnel, air dried and then dried in vacuo. The weight average molecular weight of the resulting polymer was 9000 for standard polystyrene.
example 2
[0114] Example 2: Synthesis of Matrix Polymer 2
[0115] The polymer referred to herein as "Matrix Polymer 2" or simply "Polymer 2" was prepared in the following manner. 17 g of tris-(2-carboxyethyl) isocyanurate, 23 g of tris-(2-hydroxyethyl) isocyanurate, a catalytic amount of p-toluenesulfonic acid monohydrate and 33 g of anisole were fed into the reactor middle. After the reaction was completed, the reaction solution was cooled and diluted. The polymer was precipitated by dropwise addition of a sufficient amount of isopropanol and collected by filtration in a Buchner funnel, air dried and then dried in vacuo. The weight average molecular weight of the resulting polymer was 7000 for standard polystyrene.
example 3
[0116] Example 3: Synthesis of Matrix Polymer 3
[0117] The polymer referred to herein as "Matrix Polymer 3" or simply "Polymer 3" was prepared in the following manner. 15g of N-allyl-bis(2-carboxyethyl) isocyanurate, 27g of tris-(2-hydroxyethyl) isocyanurate, and a catalytic amount of p-toluenesulfonic acid acid monohydrate, PTSA) and 30 g of anisole were fed into the reactor. After the reaction was completed, the reaction solution was cooled and diluted. The polymer was precipitated by dropwise addition of a sufficient amount of alcoholic solvent and collected by filtration in a Buchner funnel, air dried and then dried in vacuo. The weight average molecular weight of the resulting polymer was 19,000 for standard polystyrene.
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