Keto-imidazoline-2-imine ligand [N,O] bidentate nickel and palladium complex as well as preparation method and application thereof
A technology of palladium complex and imidazoline, which is applied to [N,O] bidentate nickel and palladium complex of ketone-imidazoline-2-imine ligand and the fields of preparation and application thereof, can solve the problem of high application cost, It is difficult to achieve problems such as poor tolerance of oligomers and polar monomers, and achieve the effects of strong electronegativity, improved thermal stability, and improved catalytic activity
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Embodiment 1
[0083] The preparation method of ketone-imidazoline-2-imine [N, O] bidentate nickel complex, concrete steps are as follows:
[0084] (1) preparation of ketone-imidazoline-2-imine ligand;
[0085] (1.1) Dissolve aminoacetaldehyde dimethyl acetal and O-methylisourea sulfate in water at a molar ratio of 1.5:1, react at 60°C with catalyst hydrochloric acid for 6 hours, and obtain a colorless solution, wherein hydrochloric acid and The mol ratio of O-methylisourea sulfate is 3:1; Be 2-amino-1H-imidazole hemisulfate, the productive rate is 75%, 1 H NMR (D 2 O, δ, ppm): 7.80 (s, 2H, = CH);
[0086] (1.2) React 2-amino-1H-imidazole hemisulfate in aqueous solution with sodium carbonate whose molar weight is 2 times its molar weight at room temperature for 3 hours to obtain 2-amino-1H-imidazole, an insoluble yellow-brown oil ;
[0087] (1.3) Dissolve 2-amino-1H-imidazole and iodobenzene in absolute ethanol, react for 16 hours at 80°C under the action of a catalytic system, cool to 5...
Embodiment 2
[0095] The preparation method of ketone-imidazoline-2-imine [N, O] bidentate nickel complex, concrete steps are as follows:
[0096] (1) preparation of ketone-imidazoline-2-imine ligand;
[0097] (1.1) Dissolve aminoacetaldehyde dimethyl acetal and O-methylisourea sulfate in water at a molar ratio of 1.5:1, and react for 6 hours at 60°C under the action of catalyst sulfuric acid to obtain a colorless solution, wherein sulfuric acid and The molar ratio of O-methylisourea sulfate is 3:2; that is, 2-amino-1H-imidazole hemisulfate, and the yield is 75%. 1 H NMR (D 2 O, δ, ppm): 7.80 (s, 2H, = CH);
[0098] (1.2) react 2-amino-1H-imidazole hemisulfate in an aqueous solution with sodium carbonate whose molar weight is 2.5 times its molar weight at room temperature for 3 hours to obtain 2-amino-1H-imidazole;
[0099] (1.3) Dissolve 2-amino-1H-imidazole and iodobenzene in anhydrous isopropanol, react for 16 hours at 80°C under the action of a catalytic system, cool to 50°C, drain t...
Embodiment 3
[0107] The preparation method of ketone-imidazoline-2-imine [N, O] bidentate palladium complex, concrete steps are as follows:
[0108] (1) preparation of ketone-imidazoline-2-imine ligand;
[0109] (1.1) Dissolve aminoacetaldehyde dimethyl acetal and O-methylisourea sulfate in water with a molar ratio of 1.5:1, and react for 6 hours at 60°C with catalyst nitric acid to obtain a colorless solution, wherein nitric acid and The molar ratio of O-methylisourea sulfate is 3:2; that is, 2-amino-1H-imidazole hemisulfate, and the yield is 75%. 1 H NMR (D 2 O, δ, ppm): 7.80 (s, 2H, = CH);
[0110] (1.2) react 2-amino-1H-imidazole hemisulfate in an aqueous solution with sodium carbonate whose molar weight is 3 times its molarity at room temperature for 3 hours to obtain 2-amino-1H-imidazole;
[0111] (1.3) Dissolve 2-amino-1H-imidazole and iodobenzene in anhydrous isopropanol, react for 16 hours at 80°C under the action of a catalytic system, cool to 50°C, drain the reaction solvent ...
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