Synergistic Enhancement of Aggregation-Induced Luminescent Organometallic Platinum Complex Luminescent Materials by Three Ligands
An aggregation-induced luminescence and organometallic technology, which is applied in the direction of luminescent materials, platinum-based organic compounds, platinum-group organic compounds, etc., can solve the problems of complex and difficult synthesis of phosphorescent materials and the scarcity of quantities, and achieve rich types and quantities and large scalability , Novel effect of molecular skeleton
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Embodiment 1
[0044] The organometallic platinum complex phosphorescent material Pt1 of this embodiment has a chemical formula of C 26 h 23 N 3 Pt, the structural formula is Refer to attached figure 1 , its synthesis method is:
[0045] 1.0mmol complex precursor With 1.0mmol organic monodentate ligand and 0.1 mmol of cuprous iodide, 30.0 mmol of triethylamine were put into a reaction vessel, 15 mL of methanol was added in a nitrogen atmosphere, heated to 50° C. and stirred for 8 hours, then cooled to room temperature to form a precipitate. The precipitate was obtained by suction filtration, and washed several times with deionized water, methanol and methyl tert-butyl ether. After drying the solvent, a high-purity organometallic platinum complex phosphorescent material Pt1 can be obtained with a yield of 82.2%.
[0046] Its NMR characterization data are: 1 H NMR (400MHz, CDCl 3 ,δ):9.95(d,J=5.6Hz,1H),8.56(d,J=7.2Hz,2H),7.78(t,J=7.2Hz,1H),7.65(d,J=8.0Hz,1H ), 7.55(d, J=7.6Hz, 1H)...
Embodiment 2
[0049] The organometallic platinum complex phosphorescent material Pt2 of the present embodiment has a chemical formula of C 36 h 27 N 3 Pt, the structural formula is Refer to attached figure 2 , its synthesis method is:
[0050] 1.0mmol complex precursor With 1.0mmol organic monodentate ligand and 0.1 mmol of cuprous iodide, 30.0 mmol of triethylamine were put into a reaction vessel, 15 mL of methanol was added in a nitrogen atmosphere, heated to 50° C. and stirred for 8 hours, then cooled to room temperature to form a precipitate. The precipitate was obtained by suction filtration, and washed several times with deionized water, methanol and methyl tert-butyl ether. After drying the solvent, a high-purity organometallic platinum complex phosphorescent material Pt2 can be obtained with a yield of 68.3%.
[0051] Its NMR characterization data are: 1 H NMR (400MHz, CDCl 3 ,δ):9.95(d,J=5.2Hz,1H),9.11(d,J=4.8Hz,2H),7.86(t,J=7.6Hz,1H),7.81(t,J=8.0Hz,1H ), 7.68(d, J=8....
Embodiment 3
[0054] The organometallic platinum complex phosphorescent material Pt3 of the present embodiment has a chemical formula of C 42 h 39 BN 2 Pt, the structural formula is Refer to attached image 3 , its synthesis method is:
[0055] 1.0mmol complex precursor With 1.0mmol organic monodentate ligand and 0.1 mmol of cuprous iodide, 30.0 mmol of triethylamine were put into a reaction vessel, 15 mL of methanol was added in a nitrogen atmosphere, heated to 50° C. and stirred for 8 hours, then cooled to room temperature to form a precipitate. The precipitate was obtained by suction filtration, and washed several times with deionized water, methanol and methyl tert-butyl ether. After drying the solvent, a high-purity organometallic platinum complex phosphorescent material Pt3 can be obtained with a yield of 68.8%.
[0056] Its NMR characterization data are: 1 H NMR (400MHz, CDCl 3 ,δ):9.95(d,J=5.6Hz,1H),8.90(d,J=5.2Hz,2H),7.82(t,J=7.6Hz,1H),7.73(d,J=7.6Hz,1H ),7.82(t,J=7.6H...
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