Phosphor-containing crown macromolecular hybrid nanometer material and preparation method and application thereof
A technology of nanomaterials and macromolecules, which is applied in the field of phosphorus-containing tree crown macromolecular-based hybrid nanomaterials and its preparation, can solve the problems of not finding complexed copper ions and gold ions, and achieve easy operation and separation, simple methods, and low cost. cheap effect
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Embodiment 1
[0051] (1) Dissolve lauric acid (3.64mmol) in 10mL of anhydrous dichloromethane, add EDC*HCl (3.64mmol) to activate; then add dropwise 10mL of methanol solution with tyramine (3.64mmol), and react at room temperature for 12 After hours, thin layer chromatography (TLC) was used to detect the progress of the reaction, and purification was carried out by column chromatography (dichloromethane and methanol, v:v=1:19), and finally dried under vacuum to obtain lauric acid amide.
[0052] (2) Dissolve hexachlorocyclotriphosphazene (17.25mmol) in 50mL of anhydrous tetrahydrofuran, add anhydrous potassium carbonate (172.5mmol), ice bath for 20 minutes, and add 5mL dropwise with p-hydroxybenzaldehyde (86.25mmol) ) In tetrahydrofuran, react at room temperature for 12 hours, nuclear magnetic ( 31 P NMR) to detect the progress of the reaction, and then purify by column chromatography (n-hexane and ethyl acetate, v:v=1:3), and finally vacuum dry to obtain cyclotriphosphazene AB modified with fi...
Embodiment 2
[0060] (1) Dissolve lauric acid (3.64mmol) in 10mL of anhydrous dichloromethane, add EDC*HCl (3.64mmol) to activate; then add dropwise 10mL of methanol solution with tyramine (3.64mmol), and react at room temperature for 12 After hours, thin layer chromatography (TLC) was used to detect the progress of the reaction, and purification was carried out by column chromatography (dichloromethane and methanol, v:v=1:19), and finally dried under vacuum to obtain lauric acid amide.
[0061] (2) Dissolve hexachlorocyclotriphosphazene (17.25mmol) in 50mL of anhydrous tetrahydrofuran, add anhydrous potassium carbonate (172.5mmol), ice bath for 20 minutes, and add 5mL dropwise with p-hydroxybenzaldehyde (86.25mmol) ) In tetrahydrofuran, react at room temperature for 12 hours, nuclear magnetic ( 31 P NMR) to detect the progress of the reaction, and then purify by column chromatography (n-hexane and ethyl acetate, v:v=1:3), and finally vacuum dry to obtain cyclotriphosphazene AB modified with fi...
Embodiment 3
[0069] (1) Dissolve stearic acid (3.64mmol) in 10mL of dry dichloromethane, add EDC*HCl (3.64mmol) to activate; then add dropwise 10mL of methanol solution with tyramine (3.64mmol), and react at room temperature After 12 hours, thin layer chromatography (TLC) was used to detect the progress of the reaction, and purification was carried out by column chromatography (dichloromethane and methanol, v:v=1:19), and finally dried under vacuum to obtain stearic acid amide.
[0070] (2) Dissolve hexachlorocyclotriphosphazene (17.25mmol) in 50mL of anhydrous tetrahydrofuran, add anhydrous potassium carbonate (172.5mmol), ice bath for 20 minutes, and add 5mL dropwise with p-hydroxybenzaldehyde (86.25mmol) ) In tetrahydrofuran, react at room temperature for 12 hours, nuclear magnetic ( 31 P NMR) to detect the progress of the reaction, and then purify by column chromatography (n-hexane and ethyl acetate, v:v=1:3), and finally vacuum dry to obtain cyclotriphosphazene AB modified with five p-hyd...
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