Cyclopentadienyl transition metal compounds, as polymerization catalysts
A technology based on cyclopentadienyl and transition metals, applied in metallocenes, organic chemistry, chemical instruments and methods, etc., can solve the problem of increasing the final cost of catalysts
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Embodiment 1
[0096] In this example, a stable isolatable complex was prepared by mixing 2.5 g (8.6 mmol) (2-dimethylaminoethyl) cyclopentadienyl titanium trichloride with 1.2 g (8.6 mmol) 2,6- Prepared by the reaction of lutidine-hydrogen chloride. The reaction was performed by first dissolving (2-dimethylaminoethyl)cyclopentadienyltitanium trichloride in 25 mL of dichloromethane, and then adding 2,6-lutidine-hydrogen chloride dry powder. The reaction was carried out at room temperature and continued for 15 minutes. Thereafter, an insoluble red-orange precipitate came out of solution. The red-orange precipitate was isolated by filtration, washed twice with 20 mL of dichloromethane and dried under vacuum. The yield of (2-dimethylaminoethyl)cyclopentadienyl titanium trichloride hydrochloride was 2.7 g (96%).
Embodiment 2
[0098] [ Four (3,5-bis-trifluoromethylphenyl)] sodium borate reaction and preparation. The reaction was carried out by first suspending (2-dimethylaminoethyl)cyclopentadienyl titanium trichloride hydrochloride in 20 mL of dichloromethane, and then adding [tetrakis(3,5-bistrifluoromethylbenzene Base)] sodium borate dry powder and completed. The reaction was carried out at room temperature for 1 hour. Thereafter, a fluorescent yellow solution containing NaCl precipitate was obtained. NaCl was removed by filtration and the solvent was removed from the mother liquor to give a flaky yellow solid. The solid was washed three times with 15 mL of pentane and dried under vacuum. 1.95 g (91%) were recovered to have the formula B[(3,5-CF 3 )C 6 h 3 ] 4 - [2-Me 2 N + (H)CH 2 CH 2 -C 5 h 4 ]TiCl 3 of yellow solid.
Embodiment 3
[0100] In this example, a stable isolatable complex was obtained by mixing 0.20 g (0.6 mmol) (2-dimethylaminoethyl) cyclopentadienyl titanium trichloride hydrochloride with 0.21 g (0.60 mmol) Prepared by the reaction of sodium phenyl borate. The reaction was carried out by first suspending (2-dimethylaminoethyl)cyclopentadienyltitanium trichloride hydrochloride in 15 mL of dichloromethane and then adding sodium tetraphenylborate dry powder. The reaction was carried out at room temperature for 1 hour. Thereafter, a yellow solution containing NaCl precipitate was obtained. NaCl was removed by filtration and the solvent was removed from the mother liquor to give a yellow solid. The solid was washed three times with 15 mL of pentane and dried under vacuum. 0.37 g (99%) was recovered to have the formula B (C 6 h 5 ) 4 - [2-Me 2 N + (H)CH 2 CH 2 -C 5 h 4 ]TiCl 3 of yellow solid.
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