Method and apparatus of producing organic compound
A technology of organic compounds and manufacturing methods, which is applied in the fields of indium organic compounds, platinum group organic compounds, organic chemistry, etc., and can solve the problems of unfavorable economic angles, inability to react at higher temperatures, and inability to efficiently synthesize ortho-position metallized coordination compounds and other issues, to achieve the effect of increasing the temperature
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Embodiment 1
[0041] use figure 1 The device shown, made of iridium(III) tris(2-phenylpyridine-N,O)[Ir(ppy) 3 ]Salt. Ir(ppy) 3 The synthetic reaction formula of is as follows.
[0042] Reaction 1
[0043]
[0044] 1.0 g (2.04 mmol) iridium-acetylacetone complex [Ir(acac) 3 ], 1.1g (7.10mmol) of 2-phenylpyridine and 5ml of glycerin were added into the flask to form a reaction solution, and the microwave of 2.45GHz wavelength was irradiated while nitrogen bubbling was carried out. Set the microwave output power to 300W and the temperature to 200°C. This preset temperature of 200°C is higher than the boiling point of acetylacetone of 140.4°C and lower than the boiling point (decomposition temperature) of glycerol of 290°C. The temperature of the reaction solution rises only to about 170° C. at first, and when acetylacetone, a low-boiling point component, begins to be distilled off after about 10 minutes, the temperature of the reaction solution rises.
[0045] When the temperature of...
Embodiment 2
[0053] As in Example 1, use figure 1 The manufacturing apparatus shown, the synthesis of iridium (III) three (2-phenylquinoline-N, O) [Ir (ppq) 3 ]. The reaction formula is shown below.
[0054] Reaction 2
[0055]
[0056] 1.0g (2.04mmol) of Ir(acac) 3 , 1.45g (7.10mmol) of 2-phenylquinoline and 5ml glycerin are added in the 100ml glass eggplant-shaped flask, the same as in Example 1, the irradiation output power is a microwave of 150W, and the set temperature is 200 ℃ to start the reaction. The temperature of the reaction solution initially rises only to about 170° C., rising when distilling off from acetylacetone starts. When the temperature of the reaction solution reached about 200°C, the target product was produced. After 15 minutes from the start of the reaction, the reaction was terminated, and the reaction solution was left to cool. 20ml of dichloromethane was added, only the dichloromethane layer was extracted, and purified by column chromatography (filler: ...
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