Naphthoxy mono-metallocene transition metal compound, catalyst composition containing same and application of catalyst composition
A technology of transition metals and compounds, applied in the direction of titanium organic compounds, etc., can solve the problem of low activity
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Embodiment 1
[0064] The synthesis of embodiment 1 pentamethylcyclopentadienyl-1-naphthyloxy-titanium dichloride
[0065] Put the magnetron into a dry 250 ml three-necked flask, place the reaction flask in a magnetic stirring device; vacuumize the three-necked flask and rinse it with nitrogen repeatedly three times. And add pentamethylcyclopentadienyl-titanium trichloride 0.63 grams under nitrogen atmosphere, add 20 milliliters of dry dichloromethane to dissolve, 1-naphthol 0.31 grams are dissolved in 20 milliliters of dry dichloromethane, room temperature Slowly add the above-mentioned three-neck flask under stirring, and react at room temperature for 24 hours. The solvent was removed in vacuo at room temperature to obtain a dark red solid, which was extracted with dry toluene and filtered with a diatomaceous earth filter aid to obtain a dark red toluene solution, which was frozen and crystallized at -25°C to obtain 0.71 g of dark red crystals. That is, pentamethylcyclopentadienyl-1-napht...
Embodiment 2
[0067] The synthesis of embodiment 2 cyclopentadienyl-1-naphthyloxy-titanium dichloride
[0068] Put the magnetron into a dry 250 ml three-necked flask, place the reaction flask in a magnetic stirring device; vacuumize the three-necked flask and rinse it with nitrogen repeatedly three times. And add 0.41 grams of cyclopentadienyl-titanium trichloride under nitrogen atmosphere, add 20 milliliters of dry dichloromethane to dissolve, dissolve 0.27 grams of 1-naphthol in 20 milliliters of dry dichloromethane, add slowly at room temperature The aforementioned three-neck flask was stirred and reacted at room temperature for 24 hours. The solvent was removed in vacuo at room temperature to obtain a black solid, which was extracted with dry toluene and filtered with diatomaceous earth filter aid to obtain a toluene solution, which was frozen and crystallized at -25°C to obtain 0.55 g of black-red crystals. That is cyclopentadienyl-1-naphthyloxy-titanium dichloride, and its molar yiel...
Embodiment 3
[0070] Synthesis of embodiment 3 cyclopentadienyl-(2,4-dichloro-1-naphthyloxy)-titanium dichloride
[0071] Put the magnetron into a dry 250 ml three-necked flask, place the reaction flask in a magnetic stirring device; vacuumize the three-necked flask and rinse it with nitrogen repeatedly three times. And add 0.54 grams of cyclopentadienyl-titanium trichloride under nitrogen atmosphere, add 20 milliliters of dry dichloromethane to dissolve, and dissolve 0.53 grams of 2,4-dichloro-1-naphthol in 20 milliliters of dry dichloromethane Chloromethane was slowly added into the aforementioned three-neck flask at room temperature, and reacted at room temperature for 24 hours under stirring. The solvent was removed in vacuo at room temperature to obtain a deep red solid, which was extracted with dry toluene and filtered with a diatomaceous earth filter aid to obtain a toluene solution, which was frozen and crystallized at -25°C to obtain 0.90 g of wine red crystals. That is cyclopenta...
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