Resist pattern coating agent and resist pattern forming method using same
A technology of resist pattern and coating agent, applied in the field of resist pattern formation and resist pattern coating agent, can solve the problems of reduced focus depth, high-priced exposure device, etc., and achieve the effect of simple and efficient formation
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment
[0238] The present invention will be specifically described below based on examples, but the present invention is not limited by these examples. In addition, "part" and "%" in an Example and a comparative example are a mass standard unless otherwise indicated. In addition, the measurement methods of various physical property values and the evaluation methods of each characteristic are shown below.
[0239] [Weight-average molecular weight (Mw) and number-average molecular weight (Mn)]: GPC columns manufactured by Tosoh Corporation (trade name "G2000HXL" two, trade name "G3000HXL" one, trade name "G4000HXL" one), Under the analytical conditions of flow rate: 1.0 mL / min, dissolution solvent: tetrahydrofuran, and column temperature: 40° C., it was measured by gel permeation chromatography (GPC) using monodisperse polystyrene as a standard. In addition, the degree of dispersion (Mw / Mn) was calculated from the measurement results of Mw and Mn.
[0240] [Residual ratio of low-mo...
Synthetic example 1
[0246] (Synthesis Example 1: Polymer (A-1))
[0247]Compound 53.93g (50mol%) shown in formula (L-1), compound 10.69g (10mol%) shown in formula (L-2) and compound 35.38g (40mol%) shown in formula (L-3) ) was dissolved in 200 g of 2-butanone, and 5.58 g of azobisisobutyronitrile (hereinafter referred to as "AIBN") was further added to prepare a monomer solution. A 1,000-mL three-necked flask charged with 100 g of 2-butanone was purged with nitrogen for 30 minutes, then heated to 80° C. while stirring, and the prepared monomer solution was added dropwise over 3 hours using a dropping funnel. The start of the dropwise addition was recorded as the polymerization start time, and the polymerization reaction was carried out for 6 hours. After the polymerization reaction was completed, the polymerization solution was water-cooled to below 30° C., then dropped into 2000 g of methanol, and the precipitated white powder was separated by filtration. The white powder separated by filtrati...
Synthetic example 2
[0249] (Synthesis Example 2: Polymer (A-2))
[0250] Instead of the compound represented by the formula (L-2), 39.14 g (37 mol%) of the compound represented by the formula (L-4) was used, and 50.16 g (50 mol%) of the compound represented by the formula (L-1) and A polymer (A-2) (78 g, yield 78%) was obtained in the same manner as in Synthesis Example 1 except that 10.70 g (13 mol%) of the compound represented by the formula (L-3) was used. The Mw of the obtained polymer (A-2) was 5,200, Mw / Mn was 1.62, and the remaining ratio of low molecular weight components was 0.03%. also, 13 As a result of C-NMR analysis, it has a repeating unit represented by formula (A-2), and the content ratio (mol ratio) of each repeating unit is a / b / c=50.0 / 37.0 / 13.0. The polymer (A-2) is referred to as a resin (A-2) having an acid dissociative group.
[0251]
PUM
| Property | Measurement | Unit |
|---|---|---|
| width | aaaaa | aaaaa |
Abstract
Description
Claims
Application Information
Login to View More 