A catalyst system for olefin polymerization and its application
A technology of olefin polymerization and catalyst, which is applied in the field of olefin polymerization catalysts, can solve the problems of few reports, performance degradation, catalyst activity, hydrogen modulation sensitivity and copolymerization performance parameters cannot be fully optimized, etc., to achieve increased bulk density and copolymerization unit content , improve the effect of activity
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preparation example 1
[0153] Under ice-bath conditions, 1,2-phthalic dimethyl ether (1.0 g) was added dropwise to a mixture of aqueous formaldehyde (4 mL / 38%) / 0.1 mL chloroform / concentrated hydrochloric acid (6 mL) to react, After 30 minutes, the solution became a paste and stirring was continued for 4 hours at room temperature. The solid was collected by filtration, washed with ice water, and thoroughly dried to obtain 0.5 g of compound A represented by formula (IV).
[0154]
preparation example 2
[0156] Dissolve 1,2-o-phenylenediethyl ether (3.3g) and paraformaldehyde (0.63g) in dry dichloromethane (30mL), stir under ice bath, and slowly drop into boron trifluoride ether (4.25g) , after the dropwise addition, remove the ice-water bath, stir at room temperature for 3 h, follow the reaction by TLC until the reaction is complete, stop the reaction, wash the mixture 3 times with water, separate the organic layer, spin dry the organic solvent to obtain an oil, add a small amount of acetone to dissolve the oil The substance was dissolved, and a large amount of methanol was added to it, and it was left standing in the refrigerator to precipitate a white solid. After suction filtration and thorough drying, 1.5 g of compound B represented by formula (V) was obtained.
[0157]
preparation example 3
[0159] Under ice-bath conditions, 3-methoxy-4-ethoxy-benzyl alcohol (3 g) was dissolved in 30 mL of methanol, and 15 mL of 65% perchloric acid was added dropwise under ice-bath and stirring. Under nitrogen protection, the mixture was stirred in an ice bath for 18 h. 30 mL of water was slowly added to the reaction product, followed by extraction of the organic phase with dichloromethane. The organic phase was carefully washed with aqueous sodium hydroxide solution, then with deionized water, and dried. The organic phase was thoroughly drained and purified by column chromatography to obtain 1 g of compound F represented by formula (VI).
[0160]
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