Luminescent material with cyclotriphosphazene cross-linked rare-earth complexes and method for preparing luminescent material
A rare earth complex, tripolyphosphazene technology, applied in luminescent materials, chemical instruments and methods, compounds of Group 5/15 elements of the periodic table, etc., can solve the problem of weak luminescence intensity of rare earth complexes, and achieve luminescence performance Excellent, excellent luminous performance, high luminous efficiency
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Embodiment 1
[0029] Example 1: Preparation method of tripolyphosphazene cross-linked rare earth complex luminescent material:
[0030] S1: Add 100ml of tetrahydrofuran (THF) 2.50g (7.19mmol) of hexachlorocyclotrimeric phosphazene, 7.13g (51.59mmol) of p-hydroxybenzoic acid, and 11.3g of potassium carbonate (82.30mmol) to a 250ml one-necked flask. o C under heating and stirring, condensed and refluxed for 48h.
[0031] S2: After the reaction is complete, change to a distillation device to distill off the solvent tetrahydrofuran; then dissolve the product with DMF and stir for 12 hours. After filtration, a clear filtrate was obtained. After half of the filtrate was evaporated, the product was finally reprecipitated with ethyl acetate, washed three times with ethyl acetate, and dried in vacuum for 12 hours.
[0032] S3: Add 0.8gTbCl to a 100ml three-neck flask 3 .6H 2 O and 40ml alcohol as solvent, sonicated to TbCl 3 .6H 2 O is completely dissolved, and hexa(4-formyl potassium phenoxy...
Embodiment 2
[0036] Example 2: Preparation method of tripolyphosphazene cross-linked rare earth complex luminescent material:
[0037] S1: Add 100ml of tetrahydrofuran (THF) 2.50g (7.19mmol) of hexachlorocyclotrimeric phosphazene, 7.13g (51.59mmol) of p-hydroxybenzoic acid, and 11.3g of potassium carbonate (82.30mmol) to a 250ml one-necked flask. o C under heating and stirring, condensed and refluxed for 48h.
[0038] S2: After the reaction is complete, change to a distillation device, distill off the solvent tetrahydrofuran, then dissolve the product with DMF, and stir for 12 hours. After filtration, a clear filtrate was obtained. After half of the filtrate was evaporated, the product was finally reprecipitated with ethyl acetate, washed three times with ethyl acetate, and dried in vacuo for 15 hours.
[0039] S3: Add 0.8g EuCl to a 100ml three-neck flask 3 .6H 2 O, 40ml alcohol as solvent, sonicated to EuCl3 .6H 2 O is completely dissolved, and hexa(4-formyl potassium phenoxycyclot...
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