Polymer having reactive silicon-containing group and production method therefor
A polymer and reactive technology, applied in the compound of group 4/14 elements of the periodic table, chemical instruments and methods, ester copolymer adhesives, etc., can solve the problem of increasing the crosslinking density of cured products and reducing crosslinking Density, low reactivity of dimethyl monomethoxysilyl group, etc., to achieve good reactivity
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Embodiment 1-1
[0182] [Example 1-1] Synthesis of polymer 1
[0183] In 200mL separable flask equipped with a stirrer, a reflux condenser and a thermometer was charged represented by the following average structural formula (II), a number average molecular weight of 10,450, polymerization degree m = polyacrylate compound having a leaving group of 40 100g (terminal functional group equivalent leaving group (Br) of 0.019 moles) and methacryloyloxy methyl methoxysilane 3.6 g of dimethyl (methacryloyl functional group amount of 0.019 mol), heated to 80 deg.] C . Wherein the input azobis-2-methylbutyronitrile 0.1g, stirred for 6 hours at 80 ℃. pass through 1 H-NMR measurement confirmed that a peak derived from the methacryloyl group of the starting material completely disappeared, the reaction was completed.
[0184] Reaction product obtained number average molecular weight of 10900, In addition, each molecule of the polymer introduces single alkoxysilyl base is 2.1.
[0185] [化 13]
[0186]
Embodiment 1-2
[0187] [Example 1-2] Synthesis of polymer 2
[0188] In 200mL separable flask equipped with a stirrer, a reflux condenser and a thermometer was charged represented by the following average structural formula (III), the number average molecular weight of 10,400, polymerization degree m = polyacrylate compound having a leaving group of 40 100g (terminal functional group equivalent leaving group (Br) of 0.019 moles) and methacryloyloxy methyl methoxysilane 3.6 g of dimethyl (methacryloyl functional group amount of 0.019 mol), heated to 80 deg.] C . Wherein the input azobis-2-methylbutyronitrile 0.1g, stirred for 6 hours at 80 ℃. pass through 1 H-NMR measurement confirmed that a peak derived from the methacryloyl group of the starting material completely disappeared, the reaction was completed.
[0189] Reaction product obtained number average molecular weight of 10800, In addition, each molecule of the polymer introduces single alkoxysilyl base is 2.2.
[0190] [Chemical 14]
[0191] ...
Embodiment 1-3
[0192] [Example 1-3] Synthesis of polymer 3
[0193] In 200mL separable flask equipped with a stirrer, a reflux condenser and a thermometer was charged represented by the above average structural formula (II), a number average molecular weight of 15,600, polymerization degree m = 60 having a leaving group polyacrylate compounds of 100g (terminal functional group equivalent leaving group (Br) of 0.013 moles) and methacryloyloxy methyl methoxysilane 2.4 g of dimethyl (amount of functional groups methacryloyl group 0.013 mol), heated to 80 ℃. Wherein the input azobis-2-methylbutyronitrile 0.1g, stirred for 6 hours at 80 ℃. pass through 1 H-NMR measurement confirmed that a peak derived from the methacryloyl group of the starting material completely disappeared, the reaction was completed.
[0194] Reaction product obtained number average molecular weight of 16100, In addition, each molecule of the polymer introduces single alkoxysilyl base is 2.0.
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