A catalyst, its preparation method, its composition and application
A catalyst and composition technology, applied in the field of olefin catalysis, can solve the problem of low catalytic activity and achieve the effects of high activity, good catalytic performance and high molecular weight
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Embodiment 1
[0064] A preparation method of catalyst, the steps are as follows:
[0065] (1) Dissolve 2-hydroxy-1,4-naphthoquinone and substituted aniline in n-heptane, add trifluoroacetic acid to react to obtain anilinonaphthoquinone ligands, the reaction temperature is 100°C, the time is 15h, the reaction Initially, the molar ratio of 2-hydroxy-1,4-naphthoquinone to substituted aniline was 1:1.15, and the molar ratio of trifluoroacetic acid to 2-hydroxy-1,4-naphthoquinone was 0.33:1,2-hydroxy- The concentration of 1,4-naphthoquinone in n-heptane is 0.125mol / L, and the structural formula of substituted aniline is as follows:
[0066]
[0067] In the formula, R 1 is methyl, R 2 is ethyl, R 3 is methyl, R 4 is ethyl, R 5 It is a methyl group, and after the reaction, the anilinaquinone ligands are purified by toluene recrystallization;
[0068] (2) Dissolving the anilino-naphthoquinone ligands in toluene, adding sodium hydride to react to obtain a ligand salt compound, the temperatu...
Embodiment 2
[0074] A preparation method of catalyst, the steps are as follows:
[0075] (1) Dissolve 2-hydroxy-1,4-naphthoquinone and substituted aniline in toluene, add trifluoroacetic acid to react to obtain aniline naphthoquinone ligands, the reaction temperature is 110°C, the time is 6h, when the reaction starts , the molar ratio of 2-hydroxyl-1,4-naphthoquinone to substituted aniline is 1:1, the molar ratio of trifluoroacetic acid to 2-hydroxyl-1,4-naphthoquinone is 0.32:1, 2-hydroxyl-1, The concentration of 4-naphthoquinone in toluene is 0.1mol / L, and the structural formula of substituted aniline is as shown in embodiment 1, and in the formula, R 1 is ethyl, R 2 is methyl, R 3 is ethyl, R 4 is methyl, R 5 After the reaction, the anilinaquinone ligands are purified by n-hexane extraction;
[0076] (2) Dissolving the anilinaquinone ligands in tetrahydrofuran, adding potassium hydride to react to obtain a ligand salt compound, the reaction temperature is 40°C, and the time is 1h. ...
Embodiment 3
[0080] A preparation method of catalyst, the steps are as follows:
[0081](1) Dissolve 2-hydroxy-1,4-naphthoquinone and substituted aniline in chlorobenzene, add trifluoroacetic acid to react to obtain anilino-naphthoquinone ligands, the reaction temperature is 130°C, the time is 6h, and the reaction starts , the molar ratio of 2-hydroxy-1,4-naphthoquinone to substituted aniline is 1:1.02, and the molar ratio of trifluoroacetic acid to 2-hydroxy-1,4-naphthoquinone is 0.32:1,2-hydroxy-1 , the concentration of 4-naphthoquinone in chlorobenzene is 0.11mol / L, and the structural formula of substituted aniline is as shown in embodiment 1, and in the formula, R 1 is isopropyl, R 2 is tert-butyl, R 3 is tert-butyl, R 4 is isopropyl, R 5 It is isopropyl, and after the reaction, the p-aniline ligands are purified by recrystallization from tetrahydrofuran;
[0082] (2) Aniline naphthoquinone ligands are dissolved in dichloromethane, and n-butyllithium is added to react to obtain a ...
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