Active energy ray-curable composition
A technology of active energy ray and curable composition, applied in the field of polymer composition, to achieve the effects of excellent flexibility, low viscosity and excellent coatability after curing
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[0186] Hereinafter, although an Example and a comparative example demonstrate this invention more concretely, this invention is not limited to the said Example.
[0187] In the following synthesis examples, raw materials were dried and purified by conventional methods and degassed with nitrogen, and transport and supply were performed under a nitrogen atmosphere.
[0188] [Single consumption rate]
[0189] The consumption rate of each monomer after polymerization was calculated by the following method. That is, 0.5 ml of the polymerization reaction solution taken from the polymerization system was added to 0.5 ml of methanol to prepare 1.0 ml of the mixed solution, and 0.1 ml of the obtained mixed solution was dissolved in 0.5 ml of deuterated chloroform to carry out 1 In H-NMR measurement, the peak (chemical shift value 6.08 to 6.10) derived from the proton directly linked to the carbon-carbon double bond of the (meth)acrylate used as a monomer and the peak derived from the ...
Synthetic example 1
[0215] (Process (1))
[0216] After adding 1.5 L of toluene to a 3 L flask whose interior was dried and replaced with nitrogen, 1,1,4,7,10,10-hexamethanol, which is a Lewis base, was added sequentially while stirring the solution in the flask. Triethylenetetramine 7.4ml (27.3mmol), 0.450mol / L toluene solution 63.6ml of isobutylbis(2,6-di-tert-butyl-4-methylphenoxy)aluminum as organoaluminum compound (28.6 mmol), cooled to -20°C. 20 ml (26.0 mmol) of a 1.30 mol / L cyclohexane solution of sec-butyl lithium as an organolithium compound was added thereto, and 2-(trimethylsilyloxy)ethyl methacrylate was added as a monomer at one time. Anionic polymerization was initiated with 33.6 ml of a mixture of 17 ml (78 mmol) of ester and 16.6 ml (156 mmol) of methyl methacrylate. 80 minutes after the completion of the addition of the monomers, the polymerization reaction liquid changed from the initial yellow color to colorless. Furthermore, after stirring for 20 minutes, the reaction liqu...
Synthetic example 2
[0230] (Process (1))
[0231] After adding 1.5 L of toluene to a 3 L flask whose interior was dried and replaced with nitrogen, 1,1,4,7,10,10-hexamethanol, which is a Lewis base, was added sequentially while stirring the solution in the flask. Triethylenetetramine 7.4ml (27.3mmol), 0.450mol / L toluene solution 63.6ml of isobutylbis(2,6-di-tert-butyl-4-methylphenoxy)aluminum as organoaluminum compound (28.6 mmol), cooled to -20°C. 20ml (26.0mmol) of a 1.30mol / L cyclohexane solution of sec-butyllithium as an organolithium compound was added thereto, and 1,1-dimethylpropane-1,3-diol diol as a monomer was added at one time. Anionic polymerization was initiated with 35.3 ml of a mixture of 18.7 ml (78 mmol) of methacrylate and 16.6 ml (156 mmol) of methyl methacrylate. After 80 minutes from the end of the addition of the mixture, the polymerization reaction liquid changed from the initial yellow color to colorless. Furthermore, after stirring for 20 minutes, the reaction liquid w...
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