Iridium complex as well as preparation method and application thereof
A kind of technology of iridium metal complex and application, applied in the field of iridium metal complex and preparation thereof, can solve the problems such as no report found, and achieve the effect of simple preparation method, good anti-parasitic effect, and easy-to-obtain raw materials
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[0031] A preparation method of iridium metal complex, which comprises the following steps:
[0032] Step 1. Take a 50ml round bottom flask, add 5g of meta-hydroxybenzaldehyde, dissolve it with 10ml of acetone, add 3.826g of anhydrous potassium carbonate, the solution is a pale yellow transparent solution, heat and stir at 45℃ to reflux for 10 minutes, then slowly drip Add 3.87ml of dimethyl sulfate, after reaction for 12h, spin the filtrate to dryness, add 2ml of deionized water, add 5ml of ethyl acetate for extraction, repeat the ethyl acetate extraction process 4 times, combine the ethyl acetate layer solution, add 10g of anhydrous The potassium carbonate is dried, and the solution is spin-dried to obtain m-methoxybenzaldehyde. Its structural formula is:
[0033]
[0034] Step 2. Dissolve 3g of m-methoxybenzaldehyde in 10ml of absolute ethanol, add 1.0g of 4-phenyl-3-thiosemicarbazide, reflux and stir at 65°C, react for 5h to obtain a purple solution, spin dry to 1ml, add 5ml et...
Embodiment 1
[0044] 1. Product preparation
[0045] Take a 50ml round bottom flask, add 5g of meta-hydroxybenzaldehyde, dissolve it with 10ml of acetone, add 3.826g of anhydrous potassium carbonate, the solution is a pale yellow transparent solution, heat and stir at 45℃ to reflux for 10 minutes, then slowly add disulfuric acid dropwise 3.87ml methyl ester, after 12h reaction, spin the filtrate to dryness, add 2ml deionized water, add 5ml ethyl acetate extraction, repeat the ethyl acetate extraction process 4 times, combine the ethyl acetate layer solution, add 10g anhydrous potassium carbonate to dry , Spin the solution to dryness to obtain m-methoxybenzaldehyde; dissolve 3g m-methoxybenzaldehyde in 10ml absolute ethanol, add 1.0g 4-phenyl-3-thiosemicarbazide, reflux and stir at 65℃ , React for 5 hours to obtain a purple solution, spin dry to 1ml, add 5ml ethanol and 5ml n-hexane, white crystals are precipitated, which is m-methoxybenzaldehyde 4-phenyl-3-thiosemicarbazide; weigh m-methoxy B...
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