A kind of metal iridium-triazole crystal-graphene oxide ternary nonlinear optical material and its preparation method
A technology of nonlinear optics and triazoles, applied in organic chemistry methods, chemical instruments and methods, luminescent materials, etc., to achieve good nonlinear optical absorption effects
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Embodiment 1
[0038] Step 1: Iridium dichloro bridged compound [Ir(ppy) 2 (μ-Cl)] 2 Synthesis
[0039] Iridium trichloride hydrate (350mg, 1mmol) and 2-phenylpyridine ligand (0.5ml, 2.5mmol), 45mL of ethylene glycol ether and 15mL of water were added to the flask, the flask was sealed and evacuated under nitrogen protection at 135°C Heat to reflux for 24 hours. Cooled to room temperature, vacuum filtered with a cloth funnel, the obtained precipitate was washed with ethanol and petroleum ether to remove reactants and impurities to obtain a light yellow powdery solid, which was naturally dried and weighed (395 mg, 32%).
[0040] Step 2: Synthesis of Auxiliary Ligands, Preparation of Routes figure 1 (A);
[0041] Add 10.4g (0.1mol) of dicyanopyridine powder to a 250mL flask, weigh 15g (0.3mol) (85%) of hydrazine hydrate and 10.5g (0.1mol) of hydrazine hydrochloride, add 100ml of ethylene glycol to the flask The reaction was carried out under reflux in an oil bath at 130° C. for 6 h with c...
Embodiment 2
[0047] Step 1 and step 2 are the same as in Example 1;
[0048] Step 3: Synthesis of Metal Iridium Complexes
[0049] Take 110mg of the product in step 1 and 52mg of the product obtained in step 2 and add it to a 100ml reaction flask, and add 40ml of dichloromethane and 15ml of methanol, and then add 40mg of KPF to it 6 . Nitrogen was passed through the bottle for 15 min and protected from light, the oil bath was heated to 75° C., and the reaction was stirred and refluxed for 24 h. The reaction solution was cooled and an appropriate amount of silica gel was spin-dried, followed by column chromatography purification (dichloromethane-ethanol, two bands were collected), and spin-dried to obtain 74 mg of metal iridium complex solid. The obtained metal iridium complex solid was cultured at room temperature with (acetone-n-hexane), and after 4 days, yellow needle-like crystals were obtained and single crystal structure characterization (CCD) was performed to confirm that the obtai...
Embodiment 3
[0053] Step 1 and step 2 are the same as in Example 1;
[0054] Step 3: Synthesis of Metal Iridium Complexes
[0055] Take 110mg of the product in step 1 and 52mg of the product obtained in step 2 and add it to a 100ml reaction flask, and add 40ml of dichloromethane and 15ml of methanol, and then add 40mg of KPF to it 6 . Nitrogen was passed through the bottle for 15 min, and then the oil bath was heated to 95 °C, and the reaction was stirred and refluxed for 24 h. The reaction solution was cooled and an appropriate amount of silica gel was spin-dried, and then purified by column chromatography (dichloromethane-ethanol, two bands were collected), and spin-dried to obtain 79 mg of metal iridium complex solid. The obtained metal iridium complex solid was cultured at room temperature with (acetone-n-hexane), and after 4 days, yellow needle-like crystals were obtained and single crystal structure characterization (CCD) was performed to confirm that the obtained complex was metal...
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