A kind of polysiloxane functionalized ethylene-norbornene copolymer and its preparation method
A technology of polysiloxane and norbornene, applied in the field of copolymers, can solve the problems of low copolymerization activity and low content of comonomers, and achieve the effect of excellent elongation at break
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Embodiment 1
[0068] (1) A 50mL flask with a magnetic stirrer is vacuum-filled three times to make it full of inert atmosphere, add 5mL toluene, 3.33g (27.5mmol) vinyl norbornene and 50ppm Karstedt catalyst solution (platinum The mass concentration was 2%), and the temperature was controlled at 20° C. and stirred for 2 h. Then slowly add 2.6g (27.5mmol) dimethylchlorosilane, and continue to stir the reaction for 24h. The resulting product was distilled under reduced pressure to obtain 4.8 g of a colorless oily liquid product with a yield of 81%.
[0069] (2) A 100mL flask equipped with a magnetic stirrer was vacuum-filled three times with nitrogen to fill it with an inert atmosphere. Add 4.9g (22.5mmol) hexamethylcyclotrisiloxane and 10mL tetrahydrofuran, and then add 9mL A solution of n-butyllithium / hexane (2.5M) initiated the ring-opening polymerization. The temperature was controlled at 0° C. and the reaction was stirred for 2 h, and then 4.6 g (22.5 mmol) of the chlorosilane capping a...
Embodiment 2
[0073] (1) Repeat step (1) in Example 1.
[0074] (2) A 100mL flask equipped with a magnetic stirrer was vacuum-filled three times with nitrogen to fill it with an inert atmosphere, and then 10.5g (22.5mmol) of trifluoropropylmethylcyclotrisiloxane and 10mL of tetrahydrofuran were added , and then 9 mL of n-butyllithium / hexane solution (2.5 M) was added to initiate ring-opening polymerization. The temperature was controlled at 0° C. and the reaction was stirred for 2 hours, and then 4.6 g of the chlorosilane capping agent prepared in step (1) was added, and the capping time was 24 hours. After washing with deionized water and n-hexane three times, drying with anhydrous magnesium sulfate and rotary evaporation to remove the solvent, 13.9 g of colorless liquid product was obtained, which was polytrifluoropropylmethylsiloxane functionalized norbornene monomer . The yield was 88%. It can be seen from the characterization of the hydrogen NMR spectrum that in the prepared monomer...
Embodiment 3
[0078] The preparation process is the same as in Example 2, except that the addition amount of polytrifluoropropylmethylsiloxane functionalized norbornene monomer in step (3) is 4.2g (120mmol / L), and 2.4g of the product is obtained.
[0079] From further analysis, it can be seen that the polymerization activity of the copolymerization reaction is as high as 2.88×10 7 g / (mol·h). The content of polytrifluoropropylmethylsiloxane functionalized norbornene monomer in the copolymer is 8.6 mol%. The copolymer had a weight average molecular weight of 46.9 kg / mol as determined by GPC analysis.
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