Rare earth complex with light conversion function and preparation method thereof
A technology of rare earth complexes and light conversion, applied in chemical instruments and methods, compounds containing elements of group 3/13 of the periodic table, luminescent materials, etc., to achieve high fluorescence quantum yield, good light absorption characteristics, and good light conversion characteristics Effect
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[0027] The synthetic method of rare earth complex of the present invention, its concrete steps are as follows:
[0028] Reacting the compound of formula V (VI, VII) with the compound of formula IV in an organic solvent to obtain the photoconversion rare earth complex of formula I (II, III).
[0029] The above reaction can be carried out in many organic solvents, such as methanol, ethanol, hexonitrile, acetone, tetrahydrofuran, dichloromethane, chloroform, one of n-hexane or a mixture thereof.
Embodiment 1
[0031] Embodiment 1, synthesizing the europium complex of structural formula VIII as shown in the formula (that is, Ln=Eu in the formula III, R 1 is 2-thienyl, R 2 trifluoromethyl)
[0032]
[0033] Formula VIII
[0034] Get compound IV (Ln=Eu, R 1 is 2-thienyl, R 2 Dissolve 0.05mmol of trifluoromethyl) in acetone to prepare solution A, take 0.05mmol of the ligand compound shown in formula VII and dissolve it in hot ethanol to prepare solution B, slowly add the solution of B to solution A middle. After stirring at 50°C for 1 h, the solvent was evaporated to dryness under reduced pressure to obtain 58 mg of a light yellow solid with the structure of Formula VIII.
[0035] Mass spectrometry (ESI) analysis was carried out to the light yellow solid obtained above, and the molecular ion peak M / Z=1159.99 was recorded; Elemental analysis (mass percentage content): C, 49.63% (49.70%); H, 3.45% (3.48% ); N, 2.44% (2.42%), theoretical values in brackets. NMR spectrum charact...
Embodiment 2
[0037] Embodiment 2, synthesizing the europium complex shown in the formula IX (that is, Ln=Eu in the formula III, R 1 and R 2 Both are trifluoromethyl)
[0038]
[0039] Formula IX
[0040] Take structure such as formula IV (Ln=Eu, R 1 and R 2 Dissolve 0.05mmol of the compound shown in trifluoromethyl) in acetone to prepare solution A, and dissolve 0.05mmol of the ligand compound shown in formula VII in hot ethanol to prepare solution B, slowly dissolve the solution of B Slowly added to solution A. After stirring at 50°C for 1 h, the solvent was evaporated to dryness under reduced pressure to obtain 55 mg of a light yellow solid with the structure shown in Formula IX.
[0041] Mass spectrometry (ESI) analysis was carried out to the light yellow solid obtained above, and the molecular ion peak M / Z=1117.61 was recorded; Elemental analysis (mass percentage content): C, 41.88% (41.91%); H, 2.78% (2.80% ); N, 2.49% (2.51%), theoretical values in brackets. NMR spectrum ...
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