Post-metallocene catalyst precursor, preparation method thereof, catalyst, application of catalyst, and ethylene homopolymerization method
A metallocene catalyst and catalyst technology are applied in the field of olefin coordination polymerization, which can solve the problems of complex catalyst preparation process and achieve the effects of low cost, good repeatability and high catalytic activity
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preparation example Construction
[0036] In the preparation method of catalyst precursor of the present invention, about R 1 , R 2 , R 3 , R 4 , R 5 , R 6 and R 7 And the definition of M can be reasonably selected through the above description, and will not be repeated here.
[0037] According to the preparation method of the catalyst precursor of the present invention, considering the availability of raw materials and making the prepared catalyst precursor have higher catalytic activity, preferably, M 1 For Li.
[0038] According to the preparation method of the catalyst precursor of the present invention, considering the availability of raw materials and making the prepared catalyst precursor have higher catalytic activity, preferably, X 1 、X 2 and x 3 Each independent degree is chlorine.
[0039] According to a preferred embodiment of the present invention, R 1 is trimethylsilyl; R 2 is tert-butyl; R 3 , R 4 , R 5 , R 6 and R 7 Each independently is hydrogen; M is Ti; M 1 is Li; X 1 、X 2...
preparation example 1
[0075] This preparation example is used to illustrate the preparation of the post-metallocene catalyst precursor with the structure represented by formula (II).
[0076] Dissolve 4-tert-butyl-2,6-bis(trimethylsilylacetylene)phenol (3.00mmol) in 30mL ether solvent, add n-hexane containing n-butyllithium to the solution at -78°C The solution (the concentration of n-butyllithium in the n-hexane solution is 1.67M, and the amount of n-butyllithium used is 3.00mmol) was reacted for 1 hour, returned to 25° C., and continued to react for 15 minutes. A compound having a structure represented by formula (VII) is obtained.
[0077]
[0078] At -78 ° C, the solution of the compound containing the structure shown in the formula (VII) obtained above was transferred to the titanium metal complex (3.00 mmol) containing the cyclopentadienyl group of the structure shown in the formula (VIII) through a double angle needle in ether solution (the amount of ether used is 30 mL), and reacted at ...
preparation example 2
[0083] This preparation example is used to illustrate the preparation of the post-metallocene catalyst precursor with the structure represented by formula (II).
[0084] Dissolve 4-tert-butyl-2,6-bis(trimethylsilylacetylene)phenol (3.00mmol) in 30mL of dichloromethane solvent, and add n-butyllithium to the solution at -78°C n-hexane solution (the concentration of n-butyllithium in the n-hexane solution is 1.67M, the amount of n-butyllithium used is 3.00mmol) and then reacted for 1 hour, returned to 20°C, and continued to react for 15 minutes. A compound having a structure represented by formula (VII) is obtained.
[0085] At -78°C, the solution of the compound containing the structure shown in the formula (VII) obtained above was transferred to the titanium metal complex (3.00 mmol) containing the cyclopentadienyl group of the structure shown in the formula (VIII) through a double angle needle in dichloromethane solution (the amount of dichloromethane used is 30 mL), and reac...
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