Metal organic complexes, preparation thereof, luminescent material and luminescent device
A technology of metal-organic and luminescent materials, applied in luminescent materials, organic chemistry, electric solid devices, etc., can solve the problems of low luminous efficiency, light purity and luminous brightness, reduce phosphorescence quenching, improve luminous efficiency and prolong service life Effect
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preparation Embodiment 1
[0072] This preparation example illustrates the preparation of metal-organic complexes provided by the invention.
[0073] (1) Preparation of ligand 5-cyano-2-benzothienylpyridine:
[0074] 10 mmol of 5-cyano-2-chloropyridine (purchased from Aldrich), 14 mmol of benzothiophene boronic acid (purchased from Aldrich), 0.1 mmol of tetrakis(triphenylphosphine)palladium[Pd(PPh 3 ) 4 ] (purchased from Aldrich Company), 30 millimolar sodium carbonate, 30 milliliters of toluene and 30 milliliters of water are placed in a 250 milliliter flask, stirred and mixed evenly, the pH value of the reaction system is 8, and heated under reflux in a water bath at 90 ° C for 4 Hour.
[0075] After cooling to room temperature, the organic phase was separated using a separatory funnel, the aqueous phase was extracted once with 20 ml of toluene, and then the organic phases were combined. The organic phase was washed with water until neutral, and the organic solvent toluene was desolvated under redu...
Embodiment 1
[0083] This example illustrates the preparation of the luminescent material and organic electroluminescent device provided by the present invention.
[0084] On an ITO glass substrate with a thickness of 0.5 mm, an etching solution (pure water: HCl: HNO 3 =10:20:1 (volume ratio); etchant equivalent concentration: 6.8-7.5N) to etch the ITO anode and the lattice pattern with a thickness of 200 nanometers. Then use deionized water, chloroform, acetone and methanol to clean ultrasonically (15 minutes each time), dry and store in isopropanol.
[0085] The ITO glass substrate obtained above was then treated with an ozone plasma microwave treatment system for 10 minutes.
[0086] After taking it out, spin-coat PEDOT / PSS aqueous solution at a speed of 3500rpm with a KW-4A desktop homogenizer, and dry it in vacuum at 90°C for 20 minutes to form a hole transport layer with a thickness of 40nm.
[0087] With the Ir(bt-5CN-py) that Preparation Example 1 obtains 3 Dissolve PVK in chloro...
Embodiment 2
[0097] This example illustrates the preparation of the luminescent material and organic electroluminescent device provided by the present invention.
[0098] Prepare an organic electroluminescent device according to the method of Example 1, the difference is that the thickness of the hole transport layer obtained by spin coating is 30 nanometers, and when the light-emitting layer is formed on the hole transport layer, the obtained in Example 1 will be prepared. Ir(bt-5CN-py) 3 Dissolved with PVK in chloroform solution, Ir(bt-5CN-py) 3 The weight ratio with PVK is 5:100, Ir(bt-5CN-py) 3 And the total consumption of PVK makes the solute (Ir(bt-5CN-py) in the above solution 3 The total concentration of PVK) was 1% by weight, and the solution was spin-coated on the hole transport layer to form a film at a speed of 2000 rpm to obtain a light-emitting layer with a thickness of 90 nanometers. And according to the method of Example 1, the organic electroluminescent device A2 was pr...
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Abstract
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