Composition for forming release layer, and release layer
A peeling layer and composition technology, applied in the direction of coatings, layered products, chemical instruments and methods, etc., can solve the problems of peeled layer damage, etc., and achieve the effects of increased yield, good reproducibility, and excellent solubility
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[0146] The following examples are given to illustrate the present invention in more detail, but the present invention is not limited to these examples.
[0147] [1] Abbreviation of compound
[0148] p-PDA: p-phenylenediamine
[0149] TPDA: 4,4”-diamino-p-terphenyl
[0150] TFMB: 2,2’-bis(trifluoromethyl)benzidine
[0151] BPDA: 3,3’,4,4’-Biphenyltetracarboxylic dianhydride
[0152] PMDA: pyromellitic dianhydride
[0153] DMCBDA: 1,3-Dimethylcyclobutanetetracarboxylic dianhydride
[0154] CBDA: cyclobutane tetracarboxylic dianhydride
[0155] MMA: methyl methacrylate
[0156] MAA: methacrylic acid
[0157] HEMA: 2-Hydroxyethyl methacrylate
[0158] AIBN: Azobisisobutyronitrile
[0159] CHMI: Cyclohexylmaleimide
[0160] EPOLEAD GT-401: Butane tetracarboxylate tetra(3,4-epoxycyclohexylmethyl) ester modified ε-caprolactone, manufactured by Daicel Co., Ltd.
[0161] CELLOXIDE 2021P: 3',4'-epoxycyclohexylmethyl 3,4-epoxycyclohexanecarboxylate, manufactured by Daicel Co.,...
Synthetic example S1
[0172]
[0173] 3.218 g (30 mmol) of p-PDA was dissolved in 88.2 g of NMP. BPDA 8.581g (29mmol) was added to the obtained solution, and it was made to react at 23 degreeC under nitrogen atmosphere for 24 hours. The Mw of the obtained polymer was 107,300, and the molecular weight distribution was 4.6.
Synthetic example S2
[0174]
[0175] Dissolve 20.261g (0.1875mol) of p-PDA and 12.206g (0.0469mol) of TPDA in 617.4g of NMP, cool to 15°C, add 50.112g (0.2298mol) of PMDA, and react at 50°C under a nitrogen atmosphere for 48 hours. The Mw of the obtained polymer was 82,100, and the molecular weight distribution was 2.7.
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