[N^O] type olefine polymerization catalyst containing N-naphthyl imine bitooth ligand and rear transition metal coordination and its preparation method
A late-transition metal and naphthyl imine technology, which is applied in the field of olefin polymerization catalysts and its preparation, can solve the problems of low molecular weight, insoluble products, and low catalytic activity
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Embodiment 1
[0038] Embodiment 1: the preparation of N-(1-naphthyl)-2-hydroxyl-benzaldimine:
[0039] To a solution of 17.55 mmol of 2-hydroxy-benzaldehyde in 40 mL of ethanol was added 19.76 mmol of 1-naphthylamine and 1 drop of formic acid, and stirred at room temperature for 24 hours. Then the reaction solution was concentrated, and the brown solid was filtered out, and subjected to silica gel column chromatography to obtain brown yellow solid L1. Yield: 63.2%.
Embodiment 2
[0040] Embodiment 2: the preparation of N-(1-naphthyl)-2-hydroxyl-3-tert-butyl-benzaldimine:
[0041] To a solution of 17.55 mmol of 2-hydroxy-3-tert-butyl-benzaldehyde in 40 mL of ethanol was added 19.76 mmol of 1-naphthylamine and 1 drop of formic acid, and stirred at room temperature for 24 hours. Then the reaction solution was concentrated, and the brown solid was filtered out and subjected to silica gel column chromatography to obtain brown yellow solid L2. Yield: 73.3%.
Embodiment 3
[0042] Embodiment 3: the preparation of N-(1-naphthyl)-2-hydroxyl-5-methoxy-benzaldimine:
[0043] To a solution of 17.55 mmol of 2-hydroxy-5-methoxy-benzaldehyde in 40 mL of ethanol was added 19.76 mmol of 1-naphthylamine and 1 drop of formic acid, and stirred at room temperature for 24 hours. Then the reaction solution was concentrated, and the brown solid was filtered out and subjected to silica gel column chromatography to obtain brown yellow solid L3. Yield: 68.8%.
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