Metal complex, light-emitting material and light-emitting device
A metal complex, metal technology, applied in luminescent materials, electroluminescent light sources, electrical components, etc., can solve the problems of limited production and reserves of iridium, and achieve the effect of excellent color purity and excellent characteristics
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[0303] Hereinafter, examples are given in order to further describe the present invention in detail, but the present invention is not limited by them.
Synthetic example 1
[0305] Synthesis of compound (L-1)
[0306] [chem 27]
[0307]
[0308] Weigh 2.84g (0.01mol) of 2-iodo-5-bromopyridine, 1.52g (0.0125mol) of phenylboronic acid, and 50mL of toluene in a reaction vessel, add 0.69g (0.006 mol) and 2M aqueous sodium carbonate solution (10 mL), heated and stirred at 80° C. for 10 hours under nitrogen flow. After recovering the organic layer of the reaction solution, it was washed with an aqueous sodium carbonate solution (80 mL) and saturated brine (20 mL). After drying over sodium sulfate, it was purified by silica gel column chromatography (hexane / toluene), and the solvent was distilled off to obtain 2.02 g (0.0086 mol) of compound (L-1). The yield was 86%.
[0309] LC-MS (positive) m / z: 234 ([M+H] + )
[0310] 1 H NMR (300MHz, CDCl 3 )
[0311] δ7.46(m, 3H), δ7.63(d, J=8.7Hz, 1H), δ7.87(m, 1H), δ7.96(m, 2H), δ8.74(s, 1H).
Synthetic example 2
[0313] Synthesis of Compound (L-2)
[0314] [chem 28]
[0315]
[0316] Weigh 29.49 g (0.125 mol) of p-dibromobenzene, 18.78 g (0.05 mol) of tris(n-butyl)(2-pyridyl)tin, 6.36 g (0.15 mol) of lithium chloride, and 200 mL of toluene in a reaction vessel. 1.75 g (0.0025 mol) of bis(triphenylphosphine)palladium(II) dichloride was added, and the mixture was refluxed for 7 hours under a nitrogen stream. After cooling in air, a saturated potassium fluoride aqueous solution (150 mL) was added, and the reaction solution was filtered. After toluene was distilled off, the residue was extracted with chloroform (500 mL), and washed with a 5% aqueous sodium bicarbonate solution (200 mL). After distilling off the solvent, it was purified by silica gel column chromatography (hexane / toluene: 1 / 1), and the solvent was distilled off to obtain 4.15 g (0.0177 mol) of compound (L-2). The yield is 36%.
[0317] LC-MS (positive) m / z: 234 ([M+H] + )
[0318] 1 H NMR (300MHz, CDCl 3 )
[03...
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