A kind of preparation method of end-group functionalized hyperbranched polyolefin
A polyolefin and functional polymer technology, applied in the field of polyolefin synthesis, can solve the problems of increased synthesis process, limited group types, practical application restrictions, etc., and achieve the effect of improving production capacity
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Embodiment 1
[0037] The present embodiment relates to a method for synthesizing end-group-functionalized hyperbranched polyolefin with controllable branching degree and controllable end-group type. The synthesis route is as follows: figure 1 shown, including the following steps:
[0038] Take 3-allyl-cyclooctene (1mmol in 1ml tetrahydrofuran), put it in a 2ml sample bottle, add Hoveyda-Grubbs second-generation catalyst (3.13mg, dissolved in 20μL tetrahydrofuran) and chain transfer agent cis-2 -Butene-1,4-diol (4.41mg, dissolved in 20μL tetrahydrofuran), reacted under argon for 24h (reaction temperature was 50°C), and then added vinyl ether / tetrahydrofuran solution (v:v=50%) ) 0.5ml terminates the reaction, the product structure is as figure 2 Shown: n is 8, m is 1, the conversion of monomer is 54.8%, and the degree of branching of the product is 29.9%.
Embodiment 2
[0040]The present embodiment relates to a method for synthesizing end-group-functionalized hyperbranched polyolefin with controllable branching degree and controllable end-group type. The synthesis route is as follows: figure 1 shown, including the following steps:
[0041] Take 3-allyl-cyclooctene (1mmol in 1ml tetrahydrofuran), put it in a 2ml sample bottle, add Grubbs third-generation catalyst (4.42mg, dissolve in 20μL tetrahydrofuran) and chain transfer agent cis-2-butane En-1,4-diol (4.41mg, dissolved in 20μL tetrahydrofuran), reacted under argon for 24h (reaction temperature was 25°C), and then added vinyl ether / tetrahydrofuran solution (v:v=50%) 0.5 The reaction is terminated by ml, and the product structure is as follows image 3 Shown: n is 10, m is 1, the conversion of monomer is 42.6%, and the degree of branching of the product is 14.9%.
Embodiment 3
[0043] The present embodiment relates to a method for synthesizing end-group-functionalized hyperbranched polyolefin with controllable branching degree and controllable end-group type. The synthesis route is as follows: figure 1 shown, including the following steps:
[0044] Take 3-allyl-cyclooctene (1mmol in 1ml tetrahydrofuran), put it in a 2ml sample bottle, add Grubbs second-generation catalyst (4.43mg, dissolved in 20μL tetrahydrofuran) and chain transfer agent maleic acid (17.41 mg, dissolved in 100 μL of tetrahydrofuran), react under argon for 24 h (reaction temperature is 50 °C), and then add 0.5 ml of vinyl ether / tetrahydrofuran solution (v:v=50%) to terminate the reaction, the product structure is as follows Figure 4 Shown: n is 6, m is 1, the conversion of monomer is 91.8%, and the degree of branching of the product is 15.0%.
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