A kind of orange light-emitting material and its preparation method and light-emitting method
A luminescent material, orange light technology, applied in luminescent materials, chemical instruments and methods, semiconductor/solid-state device manufacturing, etc., can solve problems such as low manufacturing cost, and achieve the effect of improving selectivity, promoting positive movement, and mild conditions
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Embodiment 1
[0022] Example 1 of the present invention provides a target product 3h (N-[(2-pyridyl)benzimidazole]methylene-bi(2-pyridyl)benzimidazole platinum (tolanylacetylene) complex) The preparation method:
[0023] (1) Synthesis of 1h: Weigh 2580mg (13.2mmol) of 2-(2-pyridine)benzimidazole and grind it into powder and add it to the flask, then add KOH 840mg (15mmol) and tetrabutylammonium bromide 110mg ( 0.3mmol), add 2 to 3 drops of ultrapure water into the flask, and stir the mixture in the flask into an off-white viscous substance, then add 50ml of CH 2 Cl 2 , after stirring and mixing evenly, after reacting at room temperature for 36 hours, the color of the mixed solution becomes light yellow, stop the reaction, heat the mixed solution to evaporate the solvent (the heating temperature is not particularly limited, as long as the solvent can be evaporated) , the remaining solute was eluted with petroleum ether and ethyl acetate at a volume ratio of 1:1, and then separated by colum...
Embodiment 2
[0033] Example 2 of the present invention provides a target product 3h (N-[(2-pyridyl)benzimidazole]methylene-bi(2-pyridyl)benzimidazole platinum (tolanylacetylene) complex) The preparation method:
[0034] (1) Synthesis of 1h: Weigh 2340mg (12mmol) of 2-(2-pyridine) benzimidazole and grind it into powder, add it to the flask, then add 728mg (13mmol) of KOH and 37mg (0.1 mmol), add 2 to 3 drops of ultrapure water to the flask, and stir the mixture in the 1h 80.4 of the flask into an off-white viscous substance, then add 30ml of CH 2 Cl 2 , after stirring and mixing evenly, after reacting at room temperature for 30 hours, the color of the mixed solution turns light yellow, stop the reaction, heat the mixed solution to evaporate the solvent, and use petroleum ether and ethyl acetate with a volume ratio of 1:1 for the remaining solute After the ester was eluted and separated by column chromatography, a white solid was obtained for 1h;
[0035] (2) Synthesis of 2h: Weigh the mg...
Embodiment 3
[0039] Example 3 of the present invention provides a target product 3h (N-[(2-pyridyl)benzimidazole]methylene-bi(2-pyridyl)benzimidazole platinum (tolanylacetylene) complex) The preparation method:
[0040] (1) Synthesis of 1h: Weigh 2925 mg (15 mmol) of 2-(2-pyridine) benzimidazole and grind it into powder, add it to the flask, then add 1008 mg (18 mmol) of KOH and 175 mg (0.5 mmol) of tetrabutylammonium bromide to the flask. mmol), add 2 to 3 drops of ultrapure water to the flask, and stir the mixture in the flask into an off-white viscous substance, then add 70ml CH to the flask 2 Cl 2 , after stirring and mixing evenly, after reacting at room temperature for 40 hours, the color of the mixed solution turns light yellow, stop the reaction, heat the mixed solution to evaporate the solvent, and use petroleum ether and ethyl acetate with a volume ratio of 1:1 for the remaining solute After the ester was eluted and separated by column chromatography, a white solid was obtained...
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