Organic metal iridium complex and application thereof
A technology of iridium complexes and organometallics, applied in indium organic compounds, platinum group organic compounds, organic chemistry, etc., can solve problems such as poor carrier transport ability, affecting product quality and commercial competitiveness, high cost, etc., to achieve The effect of maintaining the stability of the film layer, good industrialization prospects, and avoiding aggregation
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Embodiment 1
[0060] Example 1 Synthesis of Intermediate M1
[0061]
[0062] In a 250mL three-necked flask, nitrogen gas was introduced, 0.04mol of raw material A1, 150ml of THF, 0.05mol of raw material B1, 0.0004mol of tetrakis(triphenylphosphine) palladium were added, stirred, and then 0.06mol of K 2 CO 3 Aqueous solution (2M), heated to 80°C, refluxed for 10 hours, sampled and plated, the reaction was complete. Cool naturally, extract with 200ml of dichloromethane, separate layers, dry the extract with anhydrous sodium sulfate, filter, rotate the filtrate, and purify through a silica gel column to obtain intermediate M1 with a HPLC purity of 99.5% and a yield of 75.4%.
[0063] According to mass spectrometry, its molecular weight is 226.30 (C13H10N2S). The elemental analysis results are: C, 69.04; H, 4.43; N, 12.40; Theoretical values are: C, 69.00; H, 4.45; N, 12.38.
[0064] The intermediate Mn was prepared by the synthesis method of the intermediate M1, and the specific struc...
Embodiment 2
[0067] The synthesis of embodiment 2 intermediate N1
[0068]
[0069] In a 250ml three-necked flask, add 0.01mol A1, 0.025mol C1, 0.03mol sodium tert-butoxide, 1×10 -4 mol Pd 2 (dba) 3 , 1×10 -4 mol of tri-tert-butylphosphine, 150ml of toluene, heated to reflux for 24 hours, sampling plate, reaction complete, natural cooling, filtration, filtrate rotary evaporation, silica gel column to obtain the target product with a purity of 99.2% and a yield of 55.8%.
[0070] According to mass spectrometry, its molecular weight is 209.30 (C13H11N3). The elemental analysis results are: C, 74.64; H, 5.33; N, 20.10; theoretical values: C, 74.62; H, 5.30; N, 20.08.
[0071] Intermediate Nn was prepared by the synthesis method of intermediate N1, and the specific structure is shown in Table 1.
[0072] Table 1
[0073]
[0074]
Embodiment 3
[0075] Example 3 Synthesis of Compound 1
[0076]
[0077] In a 150mL three-necked flask, add 0.02mol of compound N1, 3g (0.01mol) of IrCl 3 (Iridium trichloride), 60ml of ethylene glycol ether, 30mL of distilled water, nitrogen protection, heated to 120 ° C, reflux for 24 hours, then stop the reaction, naturally cooled to room temperature. Add 80 mL of 1 mol / L dilute hydrochloric acid, stir evenly, filter, rinse the filter cake 3 times with distilled water, then rinse 2 times with absolute ethanol, and vacuum dry to obtain dark green intermediate B1 with a yield of 65.5%.
[0078] In a 150mL three-necked flask, add 0.005mol B1, 0.01mol C1, 0.015mol sodium carbonate (Na 2 CO 3 ), 100mL of ethylene glycol ether, nitrogen protection, heated to 110 ° C, reflux reaction for 20 hours, then stop the reaction, naturally cooled to room temperature. Filtration, the filter cake was rinsed 3 times with distilled water, then rinsed 2 times with absolute ethanol, then dissolved with ...
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