Phenoxazine two-dimensional covalent organic framework material and preparation method and application thereof
A covalent organic framework, phenoxazine technology, applied in luminescent materials, analytical materials, material excitation analysis, etc., can solve the problems of precursor design difficulty, few examples of COFs powder crystal, difficult crystallinity of COFs, etc., and achieve good application Prospect, high crystallinity, good thermal stability
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[0034] Another aspect of the embodiments of the present invention also provides a method for preparing a phenoxazine-based two-dimensional covalent organic framework material, which includes:
[0035] Under a protective atmosphere, react a uniformly mixed reaction system comprising 10-methylphenoxazine-2,7-diamine, aryl aldehydes, acetic acid aqueous solution and solvent at 100-150°C for 3-7 days to prepare A two-dimensional covalent organic framework based on phenoxazine was obtained.
[0036] In some more specific embodiments, the aryl aldehydes include 1,3,5-tris(4-formylphenyl)benzene, 1,3,5-tris(4-formylphenyl)triazine any of the
[0037] Further, the concentration of the aqueous acetic acid solution is 3-9 mol / L.
[0038] Further, the solvent is a high boiling point solvent with a boiling point range of 80-180°C.
[0039] Further, the solvent includes any one or both of N,N-dimethylformamide, N,N-dimethylacetamide, acetonitrile, dioxane, mesitylene, ortho-dichlorobenz...
Embodiment 1
[0058] Preparation of phenoxazine-based two-dimensional covalent organic framework material TFPB-DAPO-COF:
[0059] Add 20.4 mg of 10-methylphenoxazine-2,7-diamine, 23.4 mg of 1,3,5-tris(4-formylphenyl)benzene into a 10 mL Slack tube, then add 1 mL of acetonitrile, and sonicate After dissolving, add 0.6 mL of acetic acid aqueous solution with a concentration of 3 mol / L and 1 mL of mesitylene, then degas the reaction system in liquid nitrogen for three times of freezing-vacuum-thawing cycle, seal the reaction mixture in a constant temperature oven and heat to 120 °C And keep warm for 3 days. After the reaction was completed, it was cooled to room temperature, and the resulting mixture was centrifuged to collect the solid, which was then successively washed with N,N-dimethylformamide and tetrahydrofuran, and vacuum-dried at 80°C for 12 hours to obtain an orange powder TFPB-DAPO-COF. The yield was 98%.
Embodiment 2
[0061] Preparation of phenoxazine-based two-dimensional covalent organic framework material TFPT-DAPO-COF:
[0062] Add 20.4mg of 10-methylphenoxazine-2,7-diamine and 23.6mg of 1,3,5-benzenetricarbaldehyde into a 10mL Slack tube, then add 2mL of acetonitrile, dissolve it by ultrasonic, and add 0.6mL of 3mol / L acetic acid aqueous solution. Then the reaction system was degassed in liquid nitrogen by freezing-vacuum-thawing cycle three times. The reaction mixture was sealed in a constant temperature oil bath and heated to 120°C for 3 days. After the reaction was completed, it was cooled to room temperature, and the resulting mixture was centrifuged to collect the solid, which was then successively washed with N, N-dimethylformamide and tetrahydrofuran. Vacuum drying at 80° C. for 12 h gave reddish-brown powder TFPT-DAPO-COF with a yield of 88%.
[0063] Performance Characterization:
[0064] The phenoxazine-based two-dimensional covalent organic framework materials TFPB-DAPO-C...
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