Orange organic supermolecular polymer as well as preparation method and application thereof
A supramolecular polymer, organic technology, applied in the field of colored fluorescent materials, can solve the problems of affecting the life of the device, fluorescence quenching, easy aggregation and crystallization of the device, etc., and achieve high purity of crystal samples, strong thermal stability, and simple and efficient preparation method. Effect
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Embodiment 1
[0032] The preparation of embodiment 1 supramolecules of the present invention
[0033] Take the material according to the following specific mass or volume: H 4 pbod (21.9mg, 0.05mmol), bpep (18.0mg, 0.05mmol), CH 3 CN (3mL), H 2 O (7mL), HNO 3 (20 uL, 7.0 mol / L). Put the above material in a 25mL reaction kettle, stir for 0.5-1.5h, heat up to 100°C, react for 4 days, cool to room temperature naturally, observe massive crystals, filter them out from the mother liquor, wash with distilled water, and dry naturally at room temperature .
[0034] Select the large single crystal in the target product for X-ray single crystal diffraction test, and analyze the data to obtain its crystal structure. Each unit cell contains a crystallographically independent [H 3 pbod] - Components, a crystallographically independent [Hbpep] + component and a crystallographically independent water molecule, that is, the ratio of the amount of substances of the three components is 1:1:1, so the c...
Embodiment 2
[0039] The preparation of embodiment 2 supramolecules of the present invention
[0040] Take the material according to the following specific mass or volume: H 4 pbod (21.9mg, 0.05mmol), bpep (18.0mg, 0.05mmol), Cd (NO 3 ) 2 4H 2 O (30.8 mg, 0.1 mmol), CH 3 CN (2mL), H 2 O (8mL), HNO 3 (30 uL, 7.0 mol / L). Put the above material in a 25mL reaction kettle, stir for 0.5-1.5h, heat up to 80°C, react for 3 days, cool to room temperature naturally, and observe massive crystals, filter them, wash with distilled water, and dry at room temperature naturally.
[0041] Product X-ray powder diffraction characterization, obtains data similar to embodiment 1 (see figure 2 ). It shows that the crystal structure prepared by Example 2 does not change and the product purity is higher.
[0042] This embodiment is repeated many times, and [(H 3 pbod)(Hbpep)(H 2 O)] n The mass is kept at 30.0-35.2 mg, based on H 4 The pbod was calculated to be a yield of 73.5%-86.3%.
Embodiment 3
[0043] The preparation of embodiment 3 supramolecules of the present invention
[0044] Take the material according to the following specific mass or volume: H 4 pbod (21.9mg, 0.05mmol), bpep (18.0mg, 0.05mmol), Zn (NO 3 ) 2 ·6H 2 O (29.7 mg, 0.1 mmol), CH 3 CN (3mL), H 2 O (7mL), HNO 3 (20 uL, 7.0 mol / L). Put the above material in a 25mL reaction kettle, stir for 0.5-1.5h, heat up to 120°C, react for 4 days, cool to room temperature naturally, observe massive crystals, filter them out, wash with distilled water, and dry naturally at room temperature.
[0045] To product X-ray powder diffraction characterization, obtain data similar to embodiment 1 (see figure 2 ). It shows that the crystal structure prepared by Example 3 does not change and the product has higher purity.
[0046] This embodiment is repeated many times, and [(H 3 pbod)(Hbpep)(H 2 O)] n The mass of is kept at 33.9~38.9mg, based on H 4 The pbod was calculated to be a yield of 83.1%-95.2%.
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