NOVEL TETRAARYLBORATE COMPOUND, CATALYST COMPOSITION COMPRISING SAME, AND METHOD FOR PREPARING ETHYLENE HOMOPOLYMERS OR COPOLYMERS OF ETHYLENE AND alpha-OLEFIN BY USING SAME
A technology of tetraaryl borate and aryl borate, which is applied in the field of tetraaryl borate compounds, can solve problems such as uneven composition distribution, failure, and operation interruption, and achieve reduced consumption, high yield, and promotion of The effect of the operation
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[0186] Preferred organic solvents can be used in the preparation method of the present invention may be an aliphatic hydrocarbon-based solvent, (C3-C20) hydrocarbon, and the specific example thereof may be selected from one or both or more of the following Mixed Solvent: Based on linear aliphatic hydrocarbon solvent, such as butane, isobutane, pentane, hexane, heptane, octane, isooctane, decane, decane and dodecane; and cyclic Solvents of aliphatic hydrocarbons such as cyclopentane, methylcyclopentane, cyclohexane, and methylcyclohexane.
[0187] The organic solvents that can be used in the preparation method can be an aromatic hydrocarbon-based solvent.
[0188] Specifically, when the ethylene homopolymer is prepared, ethylene is used as a monomer, wherein the suitable ethylene pressure may be 1ATM to 1000 calm, more preferably 6 atm to 150 atm. Further, the polymerization temperature of 25 ° C to 220 ° C, preferably from 70 ° C to 220 ° C, and more preferably from 100 ° C to 220...
preparation example 1
[0205] (Preparation Example 1) Preparation of complex 1
[0206] Preparation of Compound 1-A
[0207]
[0208] (Preparation Example 1) Preparation of complex 1
[0209] Preparation of Compound 1-B
[0210]
[0211] The compound 1-A (6.00 g, 31.4 mmol) was added to a 250 mL round bottom flask under a nitrogen atmosphere, and 150 ml of anhydrous tetrahydrofuran (THF) was added thereto, and the mixture was stirred. N-tert-butyl-1-chloro-1-methyl-1-phenylsilane (7.16 g, 31.4 mmol) was added by dissolving in tetrahydrofuran (THF) (50 mL), and then the mixture was stirred at room temperature 12 Hour. The solvent was removed in vacuo and dissolved by adding n-hexane (150 mL), and then the solid was removed with a filter filled with dried celite. The solvent was removed to obtain a compound 1-b (10.8 g, yield of 91.0%, and the ratio of diastereomer) was obtained.
[0212] 1 H-NMR (500MHz, C 6 Di 6 PPM): Δ0.156 (D, 3H), 0.703-0.830 (M, 1H), 0.976 (D, 9H), 1.501-1.528 (m, 4H), 3.089-3...
Embodiment 1
[0218] N- octadecyl -N- alkylene octadecylphenyl tetrakis (pentafluorophenyl) borate [C 17 Hide 35 -C = N + (C 18 Hide 37 ) (C 6 Hide 5 ) B (C 6 Fly 5 ) 4 - ] Preparation of
[0219] Was added 3g (3.25mmol) trityl tetrakis (pentafluorophenyl) borate in a glove box 1L round bottom flask. Then, 300g of cyclohexane was added to the round bottom flask, and the mixture was stirred to prepare a yellow suspension at room temperature. To the suspension was added a solution of 1.95g (3.26mmol) as solid N, N- bis octadecylphenyl amine, and then stirred at room temperature for 30 minutes. Once the suspension solution became clear, which was used in subsequent copolymerization reactions without further separation.
[0220] 1 H-NMR (500MHz, CDCl 3 , Ppm): δ0.86-0.89 (m, 6H), 1.22-1.32 (m, 62H), 1.44-1.51 (m, 2H), 3.43-3.47 (m, 2H), 7.05-7.58 (m, 5H) , 7.64-7.68 (m, 1H).
[0221] Ethylene and 1-octene copolymerization by a continuous solution process
[0222] Using a continuous polymerization ...
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